ENST00000265909.9:c.2749G>T
MANE Select
|
ENSP00000265909.4:p.Val917Phe
|
|
ENST00000265909.8:c.2749G>T
|
ENSP00000265909.4:p.Val917Phe
|
|
ENST00000426933.6:c.253G>T
|
ENSP00000413345.2:p.Val85Phe
|
|
ENST00000526579.5:n.178-920G>T
|
|
|
ENST00000527116.5:n.511G>T
|
|
|
ENST00000528555.5:c.889G>T
|
ENSP00000435122.1:p.Val297Phe
|
|
ENST00000530330.1:n.485G>T
|
|
|
ENST00000530356.5:c.889G>T
|
ENSP00000432307.1:p.Val297Phe
|
|
ENST00000533318.5:n.1109G>T
|
|
|
ENST00000534726.5:c.469G>T
|
ENSP00000433699.1:p.Val157Phe
|
|
NM_001301089.1:c.889G>T
|
NP_001288018.1:p.Val297Phe
|
|
NM_014758.2:c.2749G>T
|
NP_055573.2:p.Val917Phe
|
|
XM_005271546.3:c.2574-920G>T
|
XP_005271603.1:n.2574-920G>T
|
|
XM_011542819.1:c.2995G>T
|
XP_011541121.1:p.Val999Phe
|
|
XM_011542820.1:c.2983G>T
|
XP_011541122.1:p.Val995Phe
|
|
XM_011542821.1:c.2875G>T
|
XP_011541123.1:p.Val959Phe
|
|
XM_011542824.1:c.2113G>T
|
XP_011541126.1:p.Val705Phe
|
|
XM_011542825.1:c.1270G>T
|
XP_011541127.1:p.Val424Phe
|
|
XM_011542826.1:c.1135G>T
|
XP_011541128.1:p.Val379Phe
|
|
XM_011542827.1:c.1015G>T
|
XP_011541129.1:p.Val339Phe
|
|
NM_001347918.1:c.2629G>T
|
NP_001334847.1:p.Val877Phe
|
|
NM_001347919.1:c.2574-920G>T
|
NP_001334848.1:n.2574-920G>T
|
|
NM_001347922.1:c.1078G>T
|
NP_001334851.1:p.Val360Phe
|
|
NM_001347923.1:c.1024G>T
|
NP_001334852.1:p.Val342Phe
|
|
NM_001347924.1:c.769G>T
|
NP_001334853.1:p.Val257Phe
|
|
NM_001347925.1:c.715G>T
|
NP_001334854.1:p.Val239Phe
|
|
NM_001347926.1:c.714-920G>T
|
NP_001334855.1:n.714-920G>T
|
|
NM_001347927.1:c.469G>T
|
NP_001334856.1:p.Val157Phe
|
|
NR_144939.1:n.3382G>T
|
|
|
XM_011542820.2:c.2983G>T
|
XP_011541122.1:p.Val995Phe
|
|
XM_011542821.3:c.2875G>T
|
XP_011541123.1:p.Val959Phe
|
|
XM_011542824.2:c.2113G>T
|
XP_011541126.1:p.Val705Phe
|
|
XM_011542825.2:c.1270G>T
|
XP_011541127.1:p.Val424Phe
|
|
XM_011542826.2:c.1135G>T
|
XP_011541128.1:p.Val379Phe
|
|
XM_024448521.1:c.2995G>T
|
XP_024304289.1:p.Val999Phe
|
|
XR_001747870.1:n.3820G>T
|
|
|
XR_001747872.1:n.3166G>T
|
|
|
XR_001747873.1:n.3480G>T
|
|
|
NM_001301089.2:c.889G>T
|
NP_001288018.1:p.Val297Phe
|
|
NM_001347918.2:c.2629G>T
|
NP_001334847.2:p.Val877Phe
|
|
NM_001347919.2:c.2574-920G>T
|
NP_001334848.2:n.2574-920G>T
|
|
NM_001347920.2:c.*21145G>T
|
NP_001334849.2:n.*21145G>T
|
|
NM_001347922.2:c.1078G>T
|
NP_001334851.2:p.Val360Phe
|
|
NM_001347923.2:c.1024G>T
|
NP_001334852.2:p.Val342Phe
|
|
NM_001347924.2:c.769G>T
|
NP_001334853.1:p.Val257Phe
|
|
NM_001347925.2:c.715G>T
|
NP_001334854.1:p.Val239Phe
|
|
NM_001347926.2:c.714-920G>T
|
NP_001334855.1:n.714-920G>T
|
|
NM_001347927.2:c.469G>T
|
NP_001334856.1:p.Val157Phe
|
|
NM_014758.3:c.2749G>T
MANE Select
|
NP_055573.3:p.Val917Phe
|
|
NR_144939.2:n.3374G>T
|
|
|