ENST00000350026.11:c.2797C>T
|
ENSP00000055163.8:p.Pro933Ser
|
|
ENST00000414678.8:c.2707C>T
|
ENSP00000412835.3:p.Pro903Ser
|
|
ENST00000637015.2:c.2797C>T
|
ENSP00000489729.2:p.Pro933Ser
|
|
ENST00000319584.11:c.811C>T
|
ENSP00000313006.7:p.Pro271Ser
|
|
ENST00000346085.10:c.2836C>T
|
ENSP00000344546.5:p.Pro946Ser
|
|
ENST00000350026.10:c.2548C>T
|
ENSP00000055163.7:p.Pro850Ser
|
|
ENST00000414678.7:c.955C>T
|
ENSP00000412835.2:p.Pro319Ser
|
|
ENST00000452544.2:n.698C>T
|
|
|
ENST00000635849.1:c.118C>T
|
ENSP00000490948.1:p.Pro40Ser
|
|
ENST00000636930.2:c.2797C>T
MANE Select
|
ENSP00000490491.2:p.Pro933Ser
|
|
ENST00000637015.1:c.36C>T
|
|
|
ENST00000637810.1:c.298C>T
|
ENSP00000489636.1:p.Pro100Ser
|
|
ENST00000637904.1:c.298C>T
|
ENSP00000490550.1:p.Pro100Ser
|
|
ENST00000647938.1:c.2587C>T
|
ENSP00000498155.1:p.Pro863Ser
|
|
ENST00000674190.1:n.1546C>T
|
|
|
ENST00000319584.10:c.814C>T
|
ENSP00000313006.6:p.Pro272Ser
|
|
ENST00000346085.9:c.2587C>T
|
ENSP00000344546.4:p.Pro863Ser
|
|
ENST00000350026.9:c.2548C>T
|
ENSP00000055163.7:p.Pro850Ser
|
|
ENST00000414678.6:c.955C>T
|
ENSP00000412835.2:p.Pro319Ser
|
|
ENST00000452544.1:n.644C>T
|
|
|
NM_017519.2:c.2548C>T
|
NP_059989.2:p.Pro850Ser
|
|
NM_020732.3:c.2587C>T
|
NP_065783.3:p.Pro863Ser
|
|
XM_005267069.3:c.2548C>T
|
XP_005267126.2:p.Pro850Ser
|
|
XM_011535984.1:c.1498C>T
|
XP_011534286.1:p.Pro500Ser
|
|
XM_011535985.1:c.1318C>T
|
XP_011534287.1:p.Pro440Ser
|
|
XM_011535986.1:c.1078C>T
|
XP_011534288.1:p.Pro360Ser
|
|
XM_011535987.1:c.697C>T
|
XP_011534289.1:p.Pro233Ser
|
|
XM_011535988.1:c.-20+15452C>T
|
XP_011534290.1:n.-20+15452C>T
|
|
NM_001346813.1:c.2548C>T
|
NP_001333742.1:p.Pro850Ser
|
|
NM_001363725.1:c.298C>T
|
NP_001350654.1:p.Pro100Ser
|
|
XM_011535984.2:c.2629C>T
|
XP_011534286.2:p.Pro877Ser
|
|
XM_011535988.3:c.-20+15452C>T
|
XP_011534290.1:n.-20+15452C>T
|
|
XM_017011103.2:c.2629C>T
|
XP_016866592.1:p.Pro877Ser
|
|
XM_017011104.1:c.2629C>T
|
XP_016866593.1:p.Pro877Ser
|
|
XM_017011105.2:c.2629C>T
|
XP_016866594.1:p.Pro877Ser
|
|
XM_017011106.2:c.2629C>T
|
XP_016866595.1:p.Pro877Ser
|
|
XM_017011107.2:c.2449C>T
|
XP_016866596.1:p.Pro817Ser
|
|
XR_002956289.1:n.2712C>T
|
|
|
NM_001363725.2:c.298C>T
|
NP_001350654.1:p.Pro100Ser
|
|
NM_001371656.1:c.2836C>T
|
NP_001358585.1:p.Pro946Ser
|
|
NM_001374820.1:c.2836C>T
|
NP_001361749.1:p.Pro946Ser
|
|
NM_001374828.1:c.2797C>T
MANE Select
|
NP_001361757.1:p.Pro933Ser
|
|
NM_017519.3:c.2797C>T
|
NP_059989.3:p.Pro933Ser
|
|