ENST00000344209.10:c.1546G>T
MANE Select
|
ENSP00000345667.5:p.Asp516Tyr
|
|
ENST00000460554.2:n.1496G>T
|
|
|
ENST00000642615.1:c.*729G>T
|
ENSP00000495499.1:n.*729G>T
|
|
ENST00000273691.7:c.1414G>T
|
ENSP00000273691.3:p.Asp472Tyr
|
|
ENST00000344209.9:c.1546G>T
|
ENSP00000345667.5:p.Asp516Tyr
|
|
ENST00000393631.5:c.1279G>T
|
ENSP00000377251.1:p.Asp427Tyr
|
|
ENST00000460554.1:n.1648G>T
|
|
|
ENST00000462014.1:c.1450G>T
|
ENSP00000419414.1:p.Asp484Tyr
|
|
NM_001199799.1:c.1546G>T
|
NP_001186728.1:p.Asp516Tyr
|
|
NM_001199800.1:c.1279G>T
|
NP_001186729.1:p.Asp427Tyr
|
|
NM_175924.3:c.1414G>T
|
NP_787120.1:p.Asp472Tyr
|
|
XM_005247389.3:c.1450G>T
|
XP_005247446.1:p.Asp484Tyr
|
|
XM_011512738.1:c.1546G>T
|
XP_011511040.1:p.Asp516Tyr
|
|
XM_011512739.1:c.1009G>T
|
XP_011511041.1:p.Asp337Tyr
|
|
XM_005247389.4:c.1450G>T
|
XP_005247446.1:p.Asp484Tyr
|
|
XM_011512738.2:c.1546G>T
|
XP_011511040.1:p.Asp516Tyr
|
|
XM_011512739.2:c.1009G>T
|
XP_011511041.1:p.Asp337Tyr
|
|
NM_001199799.2:c.1546G>T
MANE Select
|
NP_001186728.1:p.Asp516Tyr
|
|
NM_001199800.2:c.1279G>T
|
NP_001186729.1:p.Asp427Tyr
|
|
NM_175924.4:c.1414G>T
|
NP_787120.1:p.Asp472Tyr
|
|