ENST00000350026.11:c.4261C>G
|
ENSP00000055163.8:p.Pro1421Ala
|
|
ENST00000414678.8:c.4330C>G
|
ENSP00000412835.3:p.Pro1444Ala
|
|
ENST00000637015.2:c.4549C>G
|
ENSP00000489729.2:p.Pro1517Ala
|
|
ENST00000346085.10:c.4300C>G
|
ENSP00000344546.5:p.Pro1434Ala
|
|
ENST00000350026.10:c.4012C>G
|
ENSP00000055163.7:p.Pro1338Ala
|
|
ENST00000414678.7:c.2578C>G
|
ENSP00000412835.2:p.Pro860Ala
|
|
ENST00000635849.1:c.1741C>G
|
ENSP00000490948.1:p.Pro581Ala
|
|
ENST00000635957.1:c.1372C>G
|
ENSP00000490385.1:p.Pro458Ala
|
|
ENST00000636227.1:n.2883C>G
|
|
|
ENST00000636254.1:n.340C>G
|
|
|
ENST00000636930.2:c.4420C>G
MANE Select
|
ENSP00000490491.2:p.Pro1474Ala
|
|
ENST00000636940.1:n.2417C>G
|
|
|
ENST00000637015.1:c.1788C>G
|
|
|
ENST00000637568.1:c.1702C>G
|
|
|
ENST00000637741.1:n.1086C>G
|
|
|
ENST00000637810.1:c.1762C>G
|
ENSP00000489636.1:p.Pro588Ala
|
|
ENST00000637904.1:c.1921C>G
|
ENSP00000490550.1:p.Pro641Ala
|
|
ENST00000647938.1:c.4051C>G
|
ENSP00000498155.1:p.Pro1351Ala
|
|
ENST00000346085.9:c.4051C>G
|
ENSP00000344546.4:p.Pro1351Ala
|
|
ENST00000350026.9:c.4012C>G
|
ENSP00000055163.7:p.Pro1338Ala
|
|
ENST00000414678.6:c.2578C>G
|
ENSP00000412835.2:p.Pro860Ala
|
|
NM_017519.2:c.4012C>G
|
NP_059989.2:p.Pro1338Ala
|
|
NM_020732.3:c.4051C>G
|
NP_065783.3:p.Pro1351Ala
|
|
XM_005267069.3:c.4171C>G
|
XP_005267126.2:p.Pro1391Ala
|
|
XM_011535984.1:c.3250C>G
|
XP_011534286.1:p.Pro1084Ala
|
|
XM_011535985.1:c.3070C>G
|
XP_011534287.1:p.Pro1024Ala
|
|
XM_011535986.1:c.2830C>G
|
XP_011534288.1:p.Pro944Ala
|
|
XM_011535987.1:c.2449C>G
|
XP_011534289.1:p.Pro817Ala
|
|
XM_011535988.1:c.1312C>G
|
XP_011534290.1:p.Pro438Ala
|
|
NM_001346813.1:c.4171C>G
|
NP_001333742.1:p.Pro1391Ala
|
|
NM_001363725.1:c.1921C>G
|
NP_001350654.1:p.Pro641Ala
|
|
XM_011535984.2:c.4381C>G
|
XP_011534286.2:p.Pro1461Ala
|
|
XM_011535988.3:c.1312C>G
|
XP_011534290.1:p.Pro438Ala
|
|
XM_017011103.2:c.4282C>G
|
XP_016866592.1:p.Pro1428Ala
|
|
XM_017011104.1:c.4252C>G
|
XP_016866593.1:p.Pro1418Ala
|
|
XM_017011105.2:c.4222C>G
|
XP_016866594.1:p.Pro1408Ala
|
|
XM_017011106.2:c.4093C>G
|
XP_016866595.1:p.Pro1365Ala
|
|
XM_017011107.2:c.4072C>G
|
XP_016866596.1:p.Pro1358Ala
|
|
XR_002956289.1:n.4427-1857C>G
|
|
|
NM_001363725.2:c.1921C>G
|
NP_001350654.1:p.Pro641Ala
|
|
NM_001371656.1:c.4300C>G
|
NP_001358585.1:p.Pro1434Ala
|
|
NM_001374820.1:c.4300C>G
|
NP_001361749.1:p.Pro1434Ala
|
|
NM_001374828.1:c.4420C>G
MANE Select
|
NP_001361757.1:p.Pro1474Ala
|
|
NM_017519.3:c.4261C>G
|
NP_059989.3:p.Pro1421Ala
|
|