ENST00000703783.1:n.305G=
|
|
|
ENST00000703785.1:n.386G=
|
|
|
ENST00000262464.9:c.3521G=
MANE Select
|
ENSP00000262464.4:p.Cys1174=
|
|
ENST00000262464.8:c.3521G=
|
ENSP00000262464.4:p.Cys1174=
|
|
ENST00000507835.5:c.71G=
|
ENSP00000426839.1:p.Cys24=
|
|
ENST00000508053.5:c.3521G=
|
ENSP00000424571.1:p.Cys1174=
|
|
ENST00000508989.5:c.3422G=
|
ENSP00000425596.1:p.Cys1141=
|
|
ENST00000619499.4:c.3518G=
|
ENSP00000482132.1:p.Cys1173=
|
|
NM_001999.3:c.3521G=
|
NP_001990.2:p.Cys1174=
|
|
XM_017009228.2:c.3368G=
|
XP_016864717.1:p.Cys1123=
|
|
NM_001999.4:c.3521G=
MANE Select
|
NP_001990.2:p.Cys1174=
|
|