ENST00000350026.11:c.4488C>T
|
ENSP00000055163.8:p.Pro1496=
|
|
ENST00000414678.8:c.4557C>T
|
ENSP00000412835.3:p.Pro1519=
|
|
ENST00000637015.2:c.4776C>T
|
ENSP00000489729.2:p.Pro1592=
|
|
ENST00000346085.10:c.4527C>T
|
ENSP00000344546.5:p.Pro1509=
|
|
ENST00000350026.10:c.4239C>T
|
ENSP00000055163.7:p.Pro1413=
|
|
ENST00000414678.7:c.2805C>T
|
ENSP00000412835.2:p.Pro935=
|
|
ENST00000635849.1:c.1968C>T
|
ENSP00000490948.1:p.Pro656=
|
|
ENST00000635957.1:c.1599C>T
|
ENSP00000490385.1:p.Pro533=
|
|
ENST00000636227.1:n.3110C>T
|
|
|
ENST00000636254.1:n.567C>T
|
|
|
ENST00000636930.2:c.4647C>T
MANE Select
|
ENSP00000490491.2:p.Pro1549=
|
|
ENST00000636940.1:n.2644C>T
|
|
|
ENST00000637015.1:c.2015C>T
|
|
|
ENST00000637568.1:c.1929C>T
|
|
|
ENST00000637741.1:n.1313C>T
|
|
|
ENST00000637810.1:c.1989C>T
|
ENSP00000489636.1:p.Pro663=
|
|
ENST00000637904.1:c.2148C>T
|
ENSP00000490550.1:p.Pro716=
|
|
ENST00000647938.1:c.4278C>T
|
ENSP00000498155.1:p.Pro1426=
|
|
ENST00000346085.9:c.4278C>T
|
ENSP00000344546.4:p.Pro1426=
|
|
ENST00000350026.9:c.4239C>T
|
ENSP00000055163.7:p.Pro1413=
|
|
ENST00000414678.6:c.2805C>T
|
ENSP00000412835.2:p.Pro935=
|
|
NM_017519.2:c.4239C>T
|
NP_059989.2:p.Pro1413=
|
|
NM_020732.3:c.4278C>T
|
NP_065783.3:p.Pro1426=
|
|
XM_005267069.3:c.4398C>T
|
XP_005267126.2:p.Pro1466=
|
|
XM_011535984.1:c.3477C>T
|
XP_011534286.1:p.Pro1159=
|
|
XM_011535985.1:c.3297C>T
|
XP_011534287.1:p.Pro1099=
|
|
XM_011535986.1:c.3057C>T
|
XP_011534288.1:p.Pro1019=
|
|
XM_011535987.1:c.2676C>T
|
XP_011534289.1:p.Pro892=
|
|
XM_011535988.1:c.1539C>T
|
XP_011534290.1:p.Pro513=
|
|
NM_001346813.1:c.4398C>T
|
NP_001333742.1:p.Pro1466=
|
|
NM_001363725.1:c.2148C>T
|
NP_001350654.1:p.Pro716=
|
|
XM_011535984.2:c.4608C>T
|
XP_011534286.2:p.Pro1536=
|
|
XM_011535988.3:c.1539C>T
|
XP_011534290.1:p.Pro513=
|
|
XM_017011103.2:c.4509C>T
|
XP_016866592.1:p.Pro1503=
|
|
XM_017011104.1:c.4479C>T
|
XP_016866593.1:p.Pro1493=
|
|
XM_017011105.2:c.4449C>T
|
XP_016866594.1:p.Pro1483=
|
|
XM_017011106.2:c.4320C>T
|
XP_016866595.1:p.Pro1440=
|
|
XM_017011107.2:c.4299C>T
|
XP_016866596.1:p.Pro1433=
|
|
XR_002956289.1:n.4594C>T
|
|
|
NM_001363725.2:c.2148C>T
|
NP_001350654.1:p.Pro716=
|
|
NM_001371656.1:c.4527C>T
|
NP_001358585.1:p.Pro1509=
|
|
NM_001374820.1:c.4527C>T
|
NP_001361749.1:p.Pro1509=
|
|
NM_001374828.1:c.4647C>T
MANE Select
|
NP_001361757.1:p.Pro1549=
|
|
NM_017519.3:c.4488C>T
|
NP_059989.3:p.Pro1496=
|
|