ENST00000265909.9:c.2728G>T
MANE Select
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ENSP00000265909.4:p.Ala910Ser
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ENST00000265909.8:c.2728G>T
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ENSP00000265909.4:p.Ala910Ser
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ENST00000426933.6:c.232G>T
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ENSP00000413345.2:p.Ala78Ser
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ENST00000526579.5:n.178-941G>T
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ENST00000527116.5:n.490G>T
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ENST00000528555.5:c.868G>T
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ENSP00000435122.1:p.Ala290Ser
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ENST00000530330.1:n.464G>T
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ENST00000530356.5:c.868G>T
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ENSP00000432307.1:p.Ala290Ser
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ENST00000533318.5:n.1088G>T
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ENST00000534726.5:c.448G>T
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ENSP00000433699.1:p.Ala150Ser
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NM_001301089.1:c.868G>T
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NP_001288018.1:p.Ala290Ser
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NM_014758.2:c.2728G>T
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NP_055573.2:p.Ala910Ser
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XM_005271546.3:c.2574-941G>T
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XP_005271603.1:n.2574-941G>T
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XM_011542819.1:c.2974G>T
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XP_011541121.1:p.Ala992Ser
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XM_011542820.1:c.2962G>T
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XP_011541122.1:p.Ala988Ser
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XM_011542821.1:c.2854G>T
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XP_011541123.1:p.Ala952Ser
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XM_011542824.1:c.2092G>T
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XP_011541126.1:p.Ala698Ser
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XM_011542825.1:c.1249G>T
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XP_011541127.1:p.Ala417Ser
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XM_011542826.1:c.1114G>T
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XP_011541128.1:p.Ala372Ser
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XM_011542827.1:c.994G>T
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XP_011541129.1:p.Ala332Ser
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NM_001347918.1:c.2608G>T
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NP_001334847.1:p.Ala870Ser
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NM_001347919.1:c.2574-941G>T
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NP_001334848.1:n.2574-941G>T
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NM_001347922.1:c.1057G>T
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NP_001334851.1:p.Ala353Ser
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NM_001347923.1:c.1003G>T
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NP_001334852.1:p.Ala335Ser
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NM_001347924.1:c.748G>T
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NP_001334853.1:p.Ala250Ser
|
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NM_001347925.1:c.694G>T
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NP_001334854.1:p.Ala232Ser
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NM_001347926.1:c.714-941G>T
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NP_001334855.1:n.714-941G>T
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NM_001347927.1:c.448G>T
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NP_001334856.1:p.Ala150Ser
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NR_144939.1:n.3361G>T
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XM_011542820.2:c.2962G>T
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XP_011541122.1:p.Ala988Ser
|
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XM_011542821.3:c.2854G>T
|
XP_011541123.1:p.Ala952Ser
|
|
XM_011542824.2:c.2092G>T
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XP_011541126.1:p.Ala698Ser
|
|
XM_011542825.2:c.1249G>T
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XP_011541127.1:p.Ala417Ser
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XM_011542826.2:c.1114G>T
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XP_011541128.1:p.Ala372Ser
|
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XM_024448521.1:c.2974G>T
|
XP_024304289.1:p.Ala992Ser
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XR_001747870.1:n.3799G>T
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XR_001747872.1:n.3145G>T
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XR_001747873.1:n.3459G>T
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NM_001301089.2:c.868G>T
|
NP_001288018.1:p.Ala290Ser
|
|
NM_001347918.2:c.2608G>T
|
NP_001334847.2:p.Ala870Ser
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NM_001347919.2:c.2574-941G>T
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NP_001334848.2:n.2574-941G>T
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NM_001347920.2:c.*21124G>T
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NP_001334849.2:n.*21124G>T
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NM_001347922.2:c.1057G>T
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NP_001334851.2:p.Ala353Ser
|
|
NM_001347923.2:c.1003G>T
|
NP_001334852.2:p.Ala335Ser
|
|
NM_001347924.2:c.748G>T
|
NP_001334853.1:p.Ala250Ser
|
|
NM_001347925.2:c.694G>T
|
NP_001334854.1:p.Ala232Ser
|
|
NM_001347926.2:c.714-941G>T
|
NP_001334855.1:n.714-941G>T
|
|
NM_001347927.2:c.448G>T
|
NP_001334856.1:p.Ala150Ser
|
|
NM_014758.3:c.2728G>T
MANE Select
|
NP_055573.3:p.Ala910Ser
|
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NR_144939.2:n.3353G>T
|
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