ENST00000706528.1:n.1530G>T
|
|
|
ENST00000240306.5:c.649G>T
MANE Select
|
ENSP00000240306.3:p.Gly217Cys
|
|
ENST00000240306.4:c.649G>T
|
ENSP00000240306.3:p.Gly217Cys
|
|
ENST00000411890.3:c.433G>T
|
ENSP00000410622.2:p.Gly145Cys
|
|
ENST00000611342.1:c.*519G>T
|
ENSP00000480366.1:n.*519G>T
|
|
NM_001934.3:c.433G>T
|
NP_001925.2:p.Gly145Cys
|
|
NM_138281.2:c.649G>T
|
NP_612138.1:p.Gly217Cys
|
|
XM_011524459.1:c.433G>T
|
XP_011522761.1:p.Gly145Cys
|
|
XM_017024291.1:c.433G>T
|
XP_016879780.1:p.Gly145Cys
|
|
NM_138281.3:c.649G>T
MANE Select
|
NP_612138.1:p.Gly217Cys
|
|
NM_001934.4:c.433G>T
|
NP_001925.2:p.Gly145Cys
|
|