ENST00000317961.9:c.3634C>A
MANE Select
|
ENSP00000322408.4:p.Pro1212Thr
|
|
ENST00000317961.8:c.3634C>A
|
ENSP00000322408.4:p.Pro1212Thr
|
|
ENST00000382806.6:c.3463C>A
|
ENSP00000372256.2:p.Pro1155Thr
|
|
ENST00000415360.1:c.550C>A
|
ENSP00000389433.1:p.Pro184Thr
|
|
ENST00000440077.5:c.3511C>A
|
ENSP00000398543.1:p.Pro1171Thr
|
|
ENST00000469599.6:n.2232C>A
|
|
|
ENST00000492117.1:n.3526C>A
|
|
|
ENST00000541639.5:c.3727C>A
|
ENSP00000444293.1:p.Pro1243Thr
|
|
NM_001146705.1:c.3727C>A
|
NP_001140177.1:p.Pro1243Thr
|
|
NM_001146706.1:c.3463C>A
|
NP_001140178.1:p.Pro1155Thr
|
|
NM_004653.4:c.3634C>A
|
NP_004644.2:p.Pro1212Thr
|
|
XM_005262560.1:c.3499C>A
|
XP_005262617.1:p.Pro1167Thr
|
|
XM_005262561.1:c.3403C>A
|
XP_005262618.1:p.Pro1135Thr
|
|
XM_011531468.1:c.3556C>A
|
XP_011529770.1:p.Pro1186Thr
|
|
XR_244571.2:n.3922C>A
|
|
|
XR_430568.2:n.4256C>A
|
|
|
XM_005262560.3:c.3499C>A
|
XP_005262617.1:p.Pro1167Thr
|
|
XM_005262561.3:c.3403C>A
|
XP_005262618.1:p.Pro1135Thr
|
|
XM_011531468.3:c.3556C>A
|
XP_011529770.1:p.Pro1186Thr
|
|
XM_024452495.1:c.1624C>A
|
XP_024308263.1:p.Pro542Thr
|
|
XM_024452496.1:c.1390C>A
|
XP_024308264.1:p.Pro464Thr
|
|
XR_001756009.2:n.4372C>A
|
|
|
XR_001756010.2:n.4372C>A
|
|
|
XR_001756011.2:n.4237C>A
|
|
|
XR_001756012.2:n.4385C>A
|
|
|
XR_001756013.2:n.3703C>A
|
|
|
XR_002958832.1:n.3804C>A
|
|
|
XR_002958834.1:n.4028C>A
|
|
|
XR_002958835.1:n.3911C>A
|
|
|
XR_002958836.1:n.4594C>A
|
|
|
XR_002958837.1:n.4401C>A
|
|
|
XR_244571.4:n.3921C>A
|
|
|
XR_430568.4:n.4255C>A
|
|
|
NM_001146706.2:c.3463C>A
|
NP_001140178.1:p.Pro1155Thr
|
|
NM_004653.5:c.3634C>A
MANE Select
|
NP_004644.2:p.Pro1212Thr
|
|
NM_001146705.2:c.3727C>A
|
NP_001140177.1:p.Pro1243Thr
|
|