ENST00000324460.7:c.1168C>A
MANE Select
|
ENSP00000324173.6:p.Pro390Thr
|
|
ENST00000679355.1:n.1523C>A
|
|
|
ENST00000679475.1:n.1752C>A
|
|
|
ENST00000680032.1:c.1168C>A
|
ENSP00000506285.1:p.Pro390Thr
|
|
ENST00000680234.1:n.1424C>A
|
|
|
ENST00000680257.1:n.1424C>A
|
|
|
ENST00000680272.1:c.1054C>A
|
ENSP00000506097.1:p.Pro352Thr
|
|
ENST00000680494.1:n.2592C>A
|
|
|
ENST00000680640.1:n.2119C>A
|
|
|
ENST00000681045.1:n.2048C>A
|
|
|
ENST00000681424.1:n.1523C>A
|
|
|
ENST00000681540.1:n.1424C>A
|
|
|
ENST00000681544.1:n.1499C>A
|
|
|
ENST00000681675.1:n.2048C>A
|
|
|
ENST00000681774.1:n.2390C>A
|
|
|
ENST00000324460.6:c.1168C>A
|
ENSP00000324173.6:p.Pro390Thr
|
|
NM_005347.4:c.1168C>A
|
NP_005338.1:p.Pro390Thr
|
|
NM_005347.5:c.1168C>A
MANE Select
|
NP_005338.1:p.Pro390Thr
|
|