ENST00000461271.6:c.589A>T
|
ENSP00000464056.2:p.Ile197Phe
|
|
ENST00000697680.1:c.*1904A>T
|
ENSP00000513392.1:n.*1904A>T
|
|
ENST00000697681.1:c.*2101A>T
|
ENSP00000513393.1:n.*2101A>T
|
|
ENST00000697683.1:c.*1804A>T
|
ENSP00000513395.1:n.*1804A>T
|
|
ENST00000697684.1:n.1000A>T
|
|
|
ENST00000697685.1:c.*1637A>T
|
ENSP00000513396.1:n.*1637A>T
|
|
ENST00000697686.1:c.589A>T
|
ENSP00000513397.1:p.Ile197Phe
|
|
ENST00000697687.1:n.819A>T
|
|
|
ENST00000697688.1:n.986A>T
|
|
|
ENST00000697689.1:c.*1440+3263A>T
|
ENSP00000513398.1:n.*1440+3263A>T
|
|
ENST00000697690.1:c.904+3263A>T
|
ENSP00000513399.1:n.904+3263A>T
|
|
ENST00000697691.1:c.*912A>T
|
ENSP00000513400.1:n.*912A>T
|
|
ENST00000697692.1:c.*952A>T
|
ENSP00000513401.1:n.*952A>T
|
|
ENST00000697694.1:c.589A>T
|
ENSP00000513402.1:p.Ile197Phe
|
|
ENST00000697695.1:n.1547A>T
|
|
|
ENST00000337432.9:c.940A>T
MANE Select
|
ENSP00000336701.4:p.Ile314Phe
|
|
ENST00000337432.8:c.940A>T
|
ENSP00000336701.4:p.Ile314Phe
|
|
ENST00000413590.5:c.578A>T
|
|
|
ENST00000475762.5:c.*1576A>T
|
ENSP00000432421.1:n.*1576A>T
|
|
ENST00000482007.5:c.*368A>T
|
ENSP00000433332.1:n.*368A>T
|
|
ENST00000487525.5:c.*513A>T
|
ENSP00000431637.1:n.*513A>T
|
|
ENST00000578151.1:n.239+3263A>T
|
|
|
ENST00000581221.5:n.455A>T
|
|
|
ENST00000583539.5:c.940A>T
|
ENSP00000463121.1:p.Ile314Phe
|
|
ENST00000584617.5:c.662A>T
|
|
|
ENST00000584804.1:c.199+3263A>T
|
ENSP00000463658.1:n.199+3263A>T
|
|
NM_058216.2:c.940A>T
|
NP_478123.1:p.Ile314Phe
|
|
NR_103872.1:n.844A>T
|
|
|
XM_006722001.2:c.940A>T
|
XP_006722064.1:p.Ile314Phe
|
|
XM_006722002.2:c.904+3263A>T
|
XP_006722065.1:n.904+3263A>T
|
|
XM_006722004.2:c.589A>T
|
XP_006722067.1:p.Ile197Phe
|
|
XM_006722005.2:c.589A>T
|
XP_006722068.1:p.Ile197Phe
|
|
XM_011525092.1:c.589A>T
|
XP_011523394.1:p.Ile197Phe
|
|
XM_011525093.1:c.589A>T
|
XP_011523395.1:p.Ile197Phe
|
|
XM_011525094.1:c.589A>T
|
XP_011523396.1:p.Ile197Phe
|
|
XR_934513.1:n.1158A>T
|
|
|
XR_934514.1:n.1158A>T
|
|
|
XM_006722001.4:c.940A>T
|
XP_006722064.1:p.Ile314Phe
|
|
XM_006722002.4:c.904+3263A>T
|
XP_006722065.1:n.904+3263A>T
|
|
XM_006722004.3:c.589A>T
|
XP_006722067.1:p.Ile197Phe
|
|
XM_006722005.3:c.589A>T
|
XP_006722068.1:p.Ile197Phe
|
|
XM_011525092.2:c.589A>T
|
XP_011523394.1:p.Ile197Phe
|
|
XM_011525093.2:c.589A>T
|
XP_011523395.1:p.Ile197Phe
|
|
XM_011525094.2:c.589A>T
|
XP_011523396.1:p.Ile197Phe
|
|
XM_017024914.1:c.589A>T
|
XP_016880403.1:p.Ile197Phe
|
|
XM_017024915.1:c.589A>T
|
XP_016880404.1:p.Ile197Phe
|
|
XM_017024916.1:c.589A>T
|
XP_016880405.1:p.Ile197Phe
|
|
XM_017024917.1:c.589A>T
|
XP_016880406.1:p.Ile197Phe
|
|
XM_017024918.2:c.589A>T
|
XP_016880407.1:p.Ile197Phe
|
|
XM_017024919.1:c.553+3263A>T
|
XP_016880408.1:n.553+3263A>T
|
|
XR_934513.3:n.1589A>T
|
|
|
XR_934514.3:n.1589A>T
|
|
|
NM_058216.3:c.940A>T
MANE Select
|
NP_478123.1:p.Ile314Phe
|
|
NR_103872.2:n.815A>T
|
|
|