ENST00000295897.9:c.1165G>C
MANE Select
|
ENSP00000295897.4:p.Asp389His
|
|
ENST00000295897.8:c.1165G>C
|
ENSP00000295897.4:p.Asp389His
|
|
ENST00000401494.7:c.820G>C
|
ENSP00000384695.3:p.Asp274His
|
|
ENST00000415165.6:c.589G>C
|
ENSP00000401820.2:p.Asp197His
|
|
ENST00000476441.6:c.*444G>C
|
ENSP00000423727.1:n.*444G>C
|
|
ENST00000484992.1:n.485G>C
|
|
|
ENST00000503124.5:c.715G>C
|
ENSP00000421027.1:p.Asp239His
|
|
ENST00000504043.1:n.168G>C
|
|
|
ENST00000505649.5:n.851G>C
|
|
|
ENST00000509063.5:c.1165G>C
|
ENSP00000422784.1:p.Asp389His
|
|
ENST00000511370.1:c.698G>C
|
|
|
ENST00000621085.4:c.526G>C
|
ENSP00000483421.1:p.Asp176His
|
|
ENST00000621628.4:c.526G>C
|
ENSP00000480485.1:p.Asp176His
|
|
NM_000477.5:c.1165G>C
|
NP_000468.1:p.Asp389His
|
|
NM_000477.6:c.1165G>C
|
NP_000468.1:p.Asp389His
|
|
NM_000477.7:c.1165G>C
MANE Select
|
NP_000468.1:p.Asp389His
|
|