ENST00000592092.2:n.1521C>T
|
|
|
ENST00000673918.2:c.6985C>T
|
ENSP00000501283.1:p.Pro2329Ser
|
|
ENST00000674114.2:c.4592C>T
|
ENSP00000501039.2:n.4592C>T
|
|
ENST00000684977.1:c.2246C>T
|
ENSP00000509384.1:n.2246C>T
|
|
ENST00000689544.1:n.2292C>T
|
|
|
ENST00000689929.1:c.2C>T
|
|
|
ENST00000691421.1:c.2182C>T
|
ENSP00000508674.1:p.Pro728Ser
|
|
ENST00000691855.1:c.6593C>T
|
|
|
ENST00000692961.1:c.6975C>T
|
ENSP00000509289.1:p.Gly2325=
|
|
ENST00000693175.1:c.2C>T
|
|
|
ENST00000693677.1:c.796C>T
|
ENSP00000509779.1:p.Pro266Ser
|
|
ENST00000420124.4:c.7051C>T
MANE Select
|
ENSP00000398837.2:p.Pro2351Ser
|
|
ENST00000673918.1:c.6985C>T
|
ENSP00000501283.1:p.Pro2329Ser
|
|
ENST00000674114.1:c.4373C>T
|
|
|
ENST00000420124.2:c.7051C>T
|
ENSP00000398837.1:p.Pro2351Ser
|
|
ENST00000592092.1:n.431C>T
|
|
|
NM_014727.2:c.7051C>T
|
NP_055542.1:p.Pro2351Ser
|
|
XM_011527561.1:c.6985C>T
|
XP_011525863.1:p.Pro2329Ser
|
|
XM_011527562.1:c.7051C>T
|
XP_011525864.1:p.Pro2351Ser
|
|
XM_011527563.1:c.6775C>T
|
XP_011525865.1:p.Pro2259Ser
|
|
XM_011527561.2:c.6487C>T
|
XP_011525863.2:p.Pro2163Ser
|
|
XM_011527562.2:c.7051C>T
|
XP_011525864.1:p.Pro2351Ser
|
|
XM_017027544.1:c.6961C>T
|
XP_016883033.1:p.Pro2321Ser
|
|
XM_017027545.1:c.6487C>T
|
XP_016883034.1:p.Pro2163Ser
|
|
XM_017027546.1:c.4015C>T
|
XP_016883035.1:p.Pro1339Ser
|
|
NM_014727.3:c.7051C>T
MANE Select
|
NP_055542.1:p.Pro2351Ser
|
|