ENST00000696982.1:c.1084A>T
|
ENSP00000513017.1:p.Arg362Ter
|
|
ENST00000527786.7:c.1063A>T
MANE Select
|
ENSP00000433488.2:p.Arg355Ter
|
|
ENST00000281428.12:c.865A>T
|
ENSP00000281428.8:p.Arg289Ter
|
|
ENST00000344954.10:c.484A>T
|
ENSP00000339627.7:p.Arg162Ter
|
|
ENST00000429175.7:c.*985A>T
|
ENSP00000399985.3:n.*985A>T
|
|
ENST00000527786.6:c.1063A>T
|
ENSP00000433488.2:p.Arg355Ter
|
|
ENST00000528790.1:n.3646A>T
|
|
|
ENST00000534087.3:c.964A>T
|
ENSP00000432950.1:p.Arg322Ter
|
|
ENST00000608303.5:c.*455A>T
|
ENSP00000477262.1:n.*455A>T
|
|
NM_001167681.2:c.964A>T
|
NP_001161153.1:p.Arg322Ter
|
|
NM_001271010.1:c.865A>T
|
NP_001257939.1:p.Arg289Ter
|
|
NM_001271012.1:c.484A>T
|
NP_001257941.1:p.Arg162Ter
|
|
NM_002017.4:c.1063A>T
|
NP_002008.2:p.Arg355Ter
|
|
XM_011542701.1:c.964A>T
|
XP_011541003.1:p.Arg322Ter
|
|
XM_011542702.1:c.937A>T
|
XP_011541004.1:p.Arg313Ter
|
|
XM_011542701.2:c.964A>T
|
XP_011541003.1:p.Arg322Ter
|
|
XM_017017405.1:c.964A>T
|
XP_016872894.1:p.Arg322Ter
|
|
XM_017017406.1:c.964A>T
|
XP_016872895.1:p.Arg322Ter
|
|
NM_002017.5:c.1063A>T
MANE Select
|
NP_002008.2:p.Arg355Ter
|
|
NM_001167681.3:c.964A>T
|
NP_001161153.1:p.Arg322Ter
|
|
NM_001271010.2:c.865A>T
|
NP_001257939.1:p.Arg289Ter
|
|
NM_001271012.2:c.484A>T
|
NP_001257941.1:p.Arg162Ter
|
|