ENST00000356141.9:c.2283G>A
MANE Select
|
ENSP00000348460.4:p.Gly761=
|
|
ENST00000551634.6:c.2292G>A
|
ENSP00000448373.2:p.Gly764=
|
|
ENST00000680362.1:c.2183G>A
|
|
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ENST00000681323.1:c.793+3009G>A
|
|
|
ENST00000346562.6:c.2187G>A
|
ENSP00000319610.5:p.Gly729=
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|
ENST00000356141.8:c.2283G>A
|
ENSP00000348460.4:p.Gly761=
|
|
ENST00000357798.9:c.2244G>A
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ENSP00000350446.5:p.Gly748=
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|
ENST00000548645.5:c.2193G>A
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ENSP00000448916.1:p.Gly731=
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ENST00000551492.5:c.2298G>A
|
ENSP00000450392.1:p.Gly766=
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|
ENST00000551634.5:c.2205G>A
|
ENSP00000448373.1:p.Gly735=
|
|
NM_001164749.1:c.2283G>A
|
NP_001158221.1:p.Gly761=
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|
NM_001165893.1:c.2193G>A
|
NP_001159365.1:p.Gly731=
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|
NM_022123.2:c.2187G>A
|
NP_071406.1:p.Gly729=
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|
NM_173159.2:c.2244G>A
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NP_775182.1:p.Gly748=
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|
XM_005267991.2:c.2304G>A
|
XP_005268048.1:p.Gly768=
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XM_005267992.2:c.2298G>A
|
XP_005268049.1:p.Gly766=
|
|
XM_005267993.2:c.2244G>A
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XP_005268050.1:p.Gly748=
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|
XM_011537067.1:c.2334G>A
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XP_011535369.1:p.Gly778=
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XM_011537068.1:c.2325G>A
|
XP_011535370.1:p.Gly775=
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XM_011537069.1:c.2295G>A
|
XP_011535371.1:p.Gly765=
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|
XM_011537070.1:c.2238G>A
|
XP_011535372.1:p.Gly746=
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|
XM_011537071.1:c.2205G>A
|
XP_011535373.1:p.Gly735=
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|
XM_011537072.1:c.2184G>A
|
XP_011535374.1:p.Gly728=
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|
XM_011537073.1:c.1977G>A
|
XP_011535375.1:p.Gly659=
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|
XM_011537074.1:c.1977G>A
|
XP_011535376.1:p.Gly659=
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|
XM_005267991.3:c.2391G>A
|
XP_005268048.2:p.Gly797=
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|
XM_005267992.3:c.2385G>A
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XP_005268049.2:p.Gly795=
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|
XM_011537067.2:c.2334G>A
|
XP_011535369.1:p.Gly778=
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|
XM_011537069.2:c.2382G>A
|
XP_011535371.2:p.Gly794=
|
|
XM_011537070.2:c.2238G>A
|
XP_011535372.1:p.Gly746=
|
|
XM_011537071.2:c.2292G>A
|
XP_011535373.2:p.Gly764=
|
|
XM_011537072.2:c.2184G>A
|
XP_011535374.1:p.Gly728=
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|
XM_017021582.1:c.2442G>A
|
XP_016877071.1:p.Gly814=
|
|
XM_017021583.1:c.2433G>A
|
XP_016877072.1:p.Gly811=
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|
XM_017021584.1:c.2352G>A
|
XP_016877073.1:p.Gly784=
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|
XM_017021585.1:c.2301G>A
|
XP_016877074.1:p.Gly767=
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|
XM_017021586.1:c.1977G>A
|
XP_016877075.1:p.Gly659=
|
|
XM_017021587.1:c.1977G>A
|
XP_016877076.1:p.Gly659=
|
|
XM_017021588.1:c.1977G>A
|
XP_016877077.1:p.Gly659=
|
|
NM_001164749.2:c.2283G>A
MANE Select
|
NP_001158221.1:p.Gly761=
|
|
NM_001165893.2:c.2193G>A
|
NP_001159365.1:p.Gly731=
|
|
NM_022123.3:c.2187G>A
|
NP_071406.1:p.Gly729=
|
|
NM_173159.3:c.2244G>A
|
NP_775182.1:p.Gly748=
|
|
NM_001394988.1:c.2238G>A
|
NP_001381917.1:p.Gly746=
|
|
NM_001394989.1:c.2184G>A
|
NP_001381918.1:p.Gly728=
|
|