ENST00000703783.1:n.549C>G
|
|
|
ENST00000703785.1:n.630C>G
|
|
|
ENST00000262464.9:c.3765C>G
MANE Select
|
ENSP00000262464.4:p.Thr1255=
|
|
ENST00000262464.8:c.3765C>G
|
ENSP00000262464.4:p.Thr1255=
|
|
ENST00000507835.5:c.315C>G
|
ENSP00000426839.1:p.Thr105=
|
|
ENST00000508053.5:c.3765C>G
|
ENSP00000424571.1:p.Thr1255=
|
|
ENST00000508989.5:c.3666C>G
|
ENSP00000425596.1:p.Thr1222=
|
|
ENST00000619499.4:c.3762C>G
|
ENSP00000482132.1:p.Thr1254=
|
|
NM_001999.3:c.3765C>G
|
NP_001990.2:p.Thr1255=
|
|
XM_017009228.2:c.3612C>G
|
XP_016864717.1:p.Thr1204=
|
|
NM_001999.4:c.3765C>G
MANE Select
|
NP_001990.2:p.Thr1255=
|
|