ENST00000703783.1:n.185C>A
|
|
|
ENST00000703785.1:n.266C>A
|
|
|
ENST00000262464.9:c.3401C>A
MANE Select
|
ENSP00000262464.4:p.Thr1134Lys
|
|
ENST00000262464.8:c.3401C>A
|
ENSP00000262464.4:p.Thr1134Lys
|
|
ENST00000507835.5:c.-50C>A
|
ENSP00000426839.1:n.-50C>A
|
|
ENST00000508053.5:c.3401C>A
|
ENSP00000424571.1:p.Thr1134Lys
|
|
ENST00000508989.5:c.3302C>A
|
ENSP00000425596.1:p.Thr1101Lys
|
|
ENST00000619499.4:c.3398C>A
|
ENSP00000482132.1:p.Thr1133Lys
|
|
NM_001999.3:c.3401C>A
|
NP_001990.2:p.Thr1134Lys
|
|
XM_017009228.2:c.3248C>A
|
XP_016864717.1:p.Thr1083Lys
|
|
NM_001999.4:c.3401C>A
MANE Select
|
NP_001990.2:p.Thr1134Lys
|
|