ENST00000350026.11:c.4251A>G
|
ENSP00000055163.8:p.Pro1417=
|
|
ENST00000414678.8:c.4320A>G
|
ENSP00000412835.3:p.Pro1440=
|
|
ENST00000637015.2:c.4539A>G
|
ENSP00000489729.2:p.Pro1513=
|
|
ENST00000346085.10:c.4290A>G
|
ENSP00000344546.5:p.Pro1430=
|
|
ENST00000350026.10:c.4002A>G
|
ENSP00000055163.7:p.Pro1334=
|
|
ENST00000414678.7:c.2568A>G
|
ENSP00000412835.2:p.Pro856=
|
|
ENST00000635849.1:c.1731A>G
|
ENSP00000490948.1:p.Pro577=
|
|
ENST00000635957.1:c.1362A>G
|
ENSP00000490385.1:p.Pro454=
|
|
ENST00000636227.1:n.2873A>G
|
|
|
ENST00000636254.1:n.330A>G
|
|
|
ENST00000636930.2:c.4410A>G
MANE Select
|
ENSP00000490491.2:p.Pro1470=
|
|
ENST00000636940.1:n.2407A>G
|
|
|
ENST00000637015.1:c.1778A>G
|
|
|
ENST00000637568.1:c.1692A>G
|
|
|
ENST00000637741.1:n.1076A>G
|
|
|
ENST00000637810.1:c.1752A>G
|
ENSP00000489636.1:p.Pro584=
|
|
ENST00000637904.1:c.1911A>G
|
ENSP00000490550.1:p.Pro637=
|
|
ENST00000647938.1:c.4041A>G
|
ENSP00000498155.1:p.Pro1347=
|
|
ENST00000346085.9:c.4041A>G
|
ENSP00000344546.4:p.Pro1347=
|
|
ENST00000350026.9:c.4002A>G
|
ENSP00000055163.7:p.Pro1334=
|
|
ENST00000414678.6:c.2568A>G
|
ENSP00000412835.2:p.Pro856=
|
|
NM_017519.2:c.4002A>G
|
NP_059989.2:p.Pro1334=
|
|
NM_020732.3:c.4041A>G
|
NP_065783.3:p.Pro1347=
|
|
XM_005267069.3:c.4161A>G
|
XP_005267126.2:p.Pro1387=
|
|
XM_011535984.1:c.3240A>G
|
XP_011534286.1:p.Pro1080=
|
|
XM_011535985.1:c.3060A>G
|
XP_011534287.1:p.Pro1020=
|
|
XM_011535986.1:c.2820A>G
|
XP_011534288.1:p.Pro940=
|
|
XM_011535987.1:c.2439A>G
|
XP_011534289.1:p.Pro813=
|
|
XM_011535988.1:c.1302A>G
|
XP_011534290.1:p.Pro434=
|
|
NM_001346813.1:c.4161A>G
|
NP_001333742.1:p.Pro1387=
|
|
NM_001363725.1:c.1911A>G
|
NP_001350654.1:p.Pro637=
|
|
XM_011535984.2:c.4371A>G
|
XP_011534286.2:p.Pro1457=
|
|
XM_011535988.3:c.1302A>G
|
XP_011534290.1:p.Pro434=
|
|
XM_017011103.2:c.4272A>G
|
XP_016866592.1:p.Pro1424=
|
|
XM_017011104.1:c.4242A>G
|
XP_016866593.1:p.Pro1414=
|
|
XM_017011105.2:c.4212A>G
|
XP_016866594.1:p.Pro1404=
|
|
XM_017011106.2:c.4083A>G
|
XP_016866595.1:p.Pro1361=
|
|
XM_017011107.2:c.4062A>G
|
XP_016866596.1:p.Pro1354=
|
|
XR_002956289.1:n.4427-1867A>G
|
|
|
NM_001363725.2:c.1911A>G
|
NP_001350654.1:p.Pro637=
|
|
NM_001371656.1:c.4290A>G
|
NP_001358585.1:p.Pro1430=
|
|
NM_001374820.1:c.4290A>G
|
NP_001361749.1:p.Pro1430=
|
|
NM_001374828.1:c.4410A>G
MANE Select
|
NP_001361757.1:p.Pro1470=
|
|
NM_017519.3:c.4251A>G
|
NP_059989.3:p.Pro1417=
|
|