ENST00000673918.2:c.4996C>T
|
ENSP00000501283.1:p.Leu1666Phe
|
|
ENST00000674114.2:c.2603C>T
|
ENSP00000501039.2:n.2603C>T
|
|
ENST00000684977.1:c.280C>T
|
ENSP00000509384.1:p.Leu94Phe
|
|
ENST00000685168.1:c.488C>T
|
|
|
ENST00000689544.1:n.215C>T
|
|
|
ENST00000691421.1:c.283C>T
|
ENSP00000508674.1:p.Leu95Phe
|
|
ENST00000691855.1:c.4604C>T
|
|
|
ENST00000692961.1:c.5062C>T
|
ENSP00000509289.1:p.Leu1688Phe
|
|
ENST00000420124.4:c.5062C>T
MANE Select
|
ENSP00000398837.2:p.Leu1688Phe
|
|
ENST00000673918.1:c.4996C>T
|
ENSP00000501283.1:p.Leu1666Phe
|
|
ENST00000674114.1:c.2384C>T
|
|
|
ENST00000420124.2:c.5062C>T
|
ENSP00000398837.1:p.Leu1688Phe
|
|
NM_014727.2:c.5062C>T
|
NP_055542.1:p.Leu1688Phe
|
|
XM_011527561.1:c.4996C>T
|
XP_011525863.1:p.Leu1666Phe
|
|
XM_011527562.1:c.5062C>T
|
XP_011525864.1:p.Leu1688Phe
|
|
XM_011527563.1:c.4786C>T
|
XP_011525865.1:p.Leu1596Phe
|
|
XM_011527561.2:c.4498C>T
|
XP_011525863.2:p.Leu1500Phe
|
|
XM_011527562.2:c.5062C>T
|
XP_011525864.1:p.Leu1688Phe
|
|
XM_017027544.1:c.5062C>T
|
XP_016883033.1:p.Leu1688Phe
|
|
XM_017027545.1:c.4498C>T
|
XP_016883034.1:p.Leu1500Phe
|
|
XM_017027546.1:c.2026C>T
|
XP_016883035.1:p.Leu676Phe
|
|
NM_014727.3:c.5062C>T
MANE Select
|
NP_055542.1:p.Leu1688Phe
|
|