ENST00000673918.2:c.4968G>A
|
ENSP00000501283.1:p.Lys1656=
|
|
ENST00000674114.2:c.2575G>A
|
ENSP00000501039.2:n.2575G>A
|
|
ENST00000684977.1:c.252G>A
|
ENSP00000509384.1:p.Lys84=
|
|
ENST00000685168.1:c.460G>A
|
|
|
ENST00000689544.1:n.187G>A
|
|
|
ENST00000691421.1:c.255G>A
|
ENSP00000508674.1:p.Lys85=
|
|
ENST00000691855.1:c.4576G>A
|
|
|
ENST00000692961.1:c.5034G>A
|
ENSP00000509289.1:p.Lys1678=
|
|
ENST00000420124.4:c.5034G>A
MANE Select
|
ENSP00000398837.2:p.Lys1678=
|
|
ENST00000673918.1:c.4968G>A
|
ENSP00000501283.1:p.Lys1656=
|
|
ENST00000674114.1:c.2356G>A
|
|
|
ENST00000420124.2:c.5034G>A
|
ENSP00000398837.1:p.Lys1678=
|
|
NM_014727.2:c.5034G>A
|
NP_055542.1:p.Lys1678=
|
|
XM_011527561.1:c.4968G>A
|
XP_011525863.1:p.Lys1656=
|
|
XM_011527562.1:c.5034G>A
|
XP_011525864.1:p.Lys1678=
|
|
XM_011527563.1:c.4758G>A
|
XP_011525865.1:p.Lys1586=
|
|
XM_011527561.2:c.4470G>A
|
XP_011525863.2:p.Lys1490=
|
|
XM_011527562.2:c.5034G>A
|
XP_011525864.1:p.Lys1678=
|
|
XM_017027544.1:c.5034G>A
|
XP_016883033.1:p.Lys1678=
|
|
XM_017027545.1:c.4470G>A
|
XP_016883034.1:p.Lys1490=
|
|
XM_017027546.1:c.1998G>A
|
XP_016883035.1:p.Lys666=
|
|
NM_014727.3:c.5034G>A
MANE Select
|
NP_055542.1:p.Lys1678=
|
|