|
NM_145038.5:c.1195T>C
MANE Select
|
NP_659475.2:p.Trp399Arg
|
|
ENST00000288710.7:c.1195T>C
MANE Select
|
ENSP00000288710.2:p.Trp399Arg
|
|
NM_145038.3:c.1195T>C
|
NP_659475.2:p.Trp399Arg
|
|
NM_145038.4:c.1195T>C
|
NP_659475.2:p.Trp399Arg
|
|
ENST00000288710.6:c.1195T>C
|
ENSP00000288710.2:p.Trp399Arg
|
|
ENST00000421869.5:c.*508T>C
|
ENSP00000414375.1:n.*508T>C
|
|
ENST00000483675.1:n.796T>C
|
|
|
ENST00000649059.1:c.1041T>C
|
|
|
XM_005264637.3:c.577T>C
|
XP_005264694.1:p.Trp193Arg
|
|
XM_005264638.3:c.175T>C
|
XP_005264695.1:p.Trp59Arg
|
|
XM_017005271.1:c.175T>C
|
XP_016860760.1:p.Trp59Arg
|
|
XM_024453218.1:c.175T>C
|
XP_024308986.1:p.Trp59Arg
|