ENST00000350026.11:c.5007A>G
|
ENSP00000055163.8:p.Pro1669=
|
|
ENST00000414678.8:c.5076A>G
|
ENSP00000412835.3:p.Pro1692=
|
|
ENST00000637015.2:c.5295A>G
|
ENSP00000489729.2:p.Pro1765=
|
|
ENST00000346085.10:c.5046A>G
|
ENSP00000344546.5:p.Pro1682=
|
|
ENST00000350026.10:c.4758A>G
|
ENSP00000055163.7:p.Pro1586=
|
|
ENST00000414678.7:c.3324A>G
|
ENSP00000412835.2:p.Pro1108=
|
|
ENST00000635849.1:c.2487A>G
|
ENSP00000490948.1:p.Pro829=
|
|
ENST00000635957.1:c.2118A>G
|
ENSP00000490385.1:p.Pro706=
|
|
ENST00000636227.1:n.3629A>G
|
|
|
ENST00000636254.1:n.1086A>G
|
|
|
ENST00000636930.2:c.5166A>G
MANE Select
|
ENSP00000490491.2:p.Pro1722=
|
|
ENST00000636940.1:n.3163A>G
|
|
|
ENST00000637015.1:c.2534A>G
|
|
|
ENST00000637568.1:c.2448A>G
|
|
|
ENST00000637741.1:n.1832A>G
|
|
|
ENST00000637810.1:c.2508A>G
|
ENSP00000489636.1:p.Pro836=
|
|
ENST00000637904.1:c.2667A>G
|
ENSP00000490550.1:p.Pro889=
|
|
ENST00000647938.1:c.4797A>G
|
ENSP00000498155.1:p.Pro1599=
|
|
ENST00000346085.9:c.4797A>G
|
ENSP00000344546.4:p.Pro1599=
|
|
ENST00000350026.9:c.4758A>G
|
ENSP00000055163.7:p.Pro1586=
|
|
ENST00000414678.6:c.3324A>G
|
ENSP00000412835.2:p.Pro1108=
|
|
NM_017519.2:c.4758A>G
|
NP_059989.2:p.Pro1586=
|
|
NM_020732.3:c.4797A>G
|
NP_065783.3:p.Pro1599=
|
|
XM_005267069.3:c.4917A>G
|
XP_005267126.2:p.Pro1639=
|
|
XM_011535984.1:c.3996A>G
|
XP_011534286.1:p.Pro1332=
|
|
XM_011535985.1:c.3816A>G
|
XP_011534287.1:p.Pro1272=
|
|
XM_011535986.1:c.3576A>G
|
XP_011534288.1:p.Pro1192=
|
|
XM_011535987.1:c.3195A>G
|
XP_011534289.1:p.Pro1065=
|
|
XM_011535988.1:c.2058A>G
|
XP_011534290.1:p.Pro686=
|
|
NM_001346813.1:c.4917A>G
|
NP_001333742.1:p.Pro1639=
|
|
NM_001363725.1:c.2667A>G
|
NP_001350654.1:p.Pro889=
|
|
XM_011535984.2:c.5127A>G
|
XP_011534286.2:p.Pro1709=
|
|
XM_011535988.3:c.2058A>G
|
XP_011534290.1:p.Pro686=
|
|
XM_017011103.2:c.5028A>G
|
XP_016866592.1:p.Pro1676=
|
|
XM_017011104.1:c.4998A>G
|
XP_016866593.1:p.Pro1666=
|
|
XM_017011105.2:c.4968A>G
|
XP_016866594.1:p.Pro1656=
|
|
XM_017011106.2:c.4839A>G
|
XP_016866595.1:p.Pro1613=
|
|
XM_017011107.2:c.4818A>G
|
XP_016866596.1:p.Pro1606=
|
|
XR_002956289.1:n.5113A>G
|
|
|
NM_001363725.2:c.2667A>G
|
NP_001350654.1:p.Pro889=
|
|
NM_001371656.1:c.5046A>G
|
NP_001358585.1:p.Pro1682=
|
|
NM_001374820.1:c.5046A>G
|
NP_001361749.1:p.Pro1682=
|
|
NM_001374828.1:c.5166A>G
MANE Select
|
NP_001361757.1:p.Pro1722=
|
|
NM_017519.3:c.5007A>G
|
NP_059989.3:p.Pro1669=
|
|