ENST00000703783.1:n.946C>A
|
|
|
ENST00000703785.1:n.1027C>A
|
|
|
ENST00000262464.9:c.4162C>A
MANE Select
|
ENSP00000262464.4:p.Pro1388Thr
|
|
ENST00000262464.8:c.4162C>A
|
ENSP00000262464.4:p.Pro1388Thr
|
|
ENST00000507835.5:c.712C>A
|
ENSP00000426839.1:p.Pro238Thr
|
|
ENST00000508053.5:c.4162C>A
|
ENSP00000424571.1:p.Pro1388Thr
|
|
ENST00000508989.5:c.4063C>A
|
ENSP00000425596.1:p.Pro1355Thr
|
|
ENST00000619499.4:c.4159C>A
|
ENSP00000482132.1:p.Pro1387Thr
|
|
NM_001999.3:c.4162C>A
|
NP_001990.2:p.Pro1388Thr
|
|
XM_017009228.2:c.4009C>A
|
XP_016864717.1:p.Pro1337Thr
|
|
NM_001999.4:c.4162C>A
MANE Select
|
NP_001990.2:p.Pro1388Thr
|
|