ENST00000703783.1:n.1059T>G
|
|
|
ENST00000703785.1:n.1140T>G
|
|
|
ENST00000262464.9:c.4275T>G
MANE Select
|
ENSP00000262464.4:p.Cys1425Trp
|
|
ENST00000262464.8:c.4275T>G
|
ENSP00000262464.4:p.Cys1425Trp
|
|
ENST00000507835.5:c.825T>G
|
ENSP00000426839.1:p.Cys275Trp
|
|
ENST00000508053.5:c.4275T>G
|
ENSP00000424571.1:p.Cys1425Trp
|
|
ENST00000508989.5:c.4176T>G
|
ENSP00000425596.1:p.Cys1392Trp
|
|
ENST00000619499.4:c.4272T>G
|
ENSP00000482132.1:p.Cys1424Trp
|
|
NM_001999.3:c.4275T>G
|
NP_001990.2:p.Cys1425Trp
|
|
XM_017009228.2:c.4122T>G
|
XP_016864717.1:p.Cys1374Trp
|
|
NM_001999.4:c.4275T>G
MANE Select
|
NP_001990.2:p.Cys1425Trp
|
|