ENST00000703783.1:n.1018T>C
|
|
|
ENST00000703785.1:n.1099T>C
|
|
|
ENST00000262464.9:c.4234T>C
MANE Select
|
ENSP00000262464.4:p.Cys1412Arg
|
|
ENST00000262464.8:c.4234T>C
|
ENSP00000262464.4:p.Cys1412Arg
|
|
ENST00000507835.5:c.784T>C
|
ENSP00000426839.1:p.Cys262Arg
|
|
ENST00000508053.5:c.4234T>C
|
ENSP00000424571.1:p.Cys1412Arg
|
|
ENST00000508989.5:c.4135T>C
|
ENSP00000425596.1:p.Cys1379Arg
|
|
ENST00000619499.4:c.4231T>C
|
ENSP00000482132.1:p.Cys1411Arg
|
|
NM_001999.3:c.4234T>C
|
NP_001990.2:p.Cys1412Arg
|
|
XM_017009228.2:c.4081T>C
|
XP_016864717.1:p.Cys1361Arg
|
|
NM_001999.4:c.4234T>C
MANE Select
|
NP_001990.2:p.Cys1412Arg
|
|