ENST00000592092.2:n.805C>G
|
|
|
ENST00000673918.2:c.6433C>G
|
ENSP00000501283.1:p.Pro2145Ala
|
|
ENST00000674114.2:c.4040C>G
|
ENSP00000501039.2:n.4040C>G
|
|
ENST00000684977.1:c.1717C>G
|
ENSP00000509384.1:p.Pro573Ala
|
|
ENST00000689544.1:n.1652C>G
|
|
|
ENST00000691421.1:c.1720C>G
|
ENSP00000508674.1:p.Pro574Ala
|
|
ENST00000691855.1:c.6041C>G
|
|
|
ENST00000692961.1:c.6499C>G
|
ENSP00000509289.1:p.Pro2167Ala
|
|
ENST00000693677.1:c.705-549C>G
|
ENSP00000509779.1:n.705-549C>G
|
|
ENST00000420124.4:c.6499C>G
MANE Select
|
ENSP00000398837.2:p.Pro2167Ala
|
|
ENST00000673918.1:c.6433C>G
|
ENSP00000501283.1:p.Pro2145Ala
|
|
ENST00000674114.1:c.3821C>G
|
|
|
ENST00000420124.2:c.6499C>G
|
ENSP00000398837.1:p.Pro2167Ala
|
|
NM_014727.2:c.6499C>G
|
NP_055542.1:p.Pro2167Ala
|
|
XM_011527561.1:c.6433C>G
|
XP_011525863.1:p.Pro2145Ala
|
|
XM_011527562.1:c.6499C>G
|
XP_011525864.1:p.Pro2167Ala
|
|
XM_011527563.1:c.6223C>G
|
XP_011525865.1:p.Pro2075Ala
|
|
XM_011527561.2:c.5935C>G
|
XP_011525863.2:p.Pro1979Ala
|
|
XM_011527562.2:c.6499C>G
|
XP_011525864.1:p.Pro2167Ala
|
|
XM_017027544.1:c.6499C>G
|
XP_016883033.1:p.Pro2167Ala
|
|
XM_017027545.1:c.5935C>G
|
XP_016883034.1:p.Pro1979Ala
|
|
XM_017027546.1:c.3463C>G
|
XP_016883035.1:p.Pro1155Ala
|
|
NM_014727.3:c.6499C>G
MANE Select
|
NP_055542.1:p.Pro2167Ala
|
|