ENST00000703783.1:n.506C>A
|
|
|
ENST00000703785.1:n.587C>A
|
|
|
ENST00000262464.9:c.3722C>A
MANE Select
|
ENSP00000262464.4:p.Thr1241Lys
|
|
ENST00000262464.8:c.3722C>A
|
ENSP00000262464.4:p.Thr1241Lys
|
|
ENST00000507835.5:c.272C>A
|
ENSP00000426839.1:p.Thr91Lys
|
|
ENST00000508053.5:c.3722C>A
|
ENSP00000424571.1:p.Thr1241Lys
|
|
ENST00000508989.5:c.3623C>A
|
ENSP00000425596.1:p.Thr1208Lys
|
|
ENST00000619499.4:c.3719C>A
|
ENSP00000482132.1:p.Thr1240Lys
|
|
NM_001999.3:c.3722C>A
|
NP_001990.2:p.Thr1241Lys
|
|
XM_017009228.2:c.3569C>A
|
XP_016864717.1:p.Thr1190Lys
|
|
NM_001999.4:c.3722C>A
MANE Select
|
NP_001990.2:p.Thr1241Lys
|
|