ENST00000695651.1:n.2531G>C
|
|
|
ENST00000695653.1:c.2092G>C
|
ENSP00000512084.1:p.Asp698His
|
|
ENST00000695654.1:c.3208G>C
|
ENSP00000512085.1:p.Asp1070His
|
|
ENST00000695689.1:c.154G>C
|
ENSP00000512101.1:n.154G>C
|
|
ENST00000695690.1:n.374G>C
|
|
|
ENST00000695691.1:n.374G>C
|
|
|
ENST00000245907.11:c.4183G>C
MANE Select
|
ENSP00000245907.4:p.Asp1395His
|
|
ENST00000245907.10:c.4183G>C
|
ENSP00000245907.4:p.Asp1395His
|
|
ENST00000596548.1:c.304G>C
|
ENSP00000469744.1:p.Asp102His
|
|
ENST00000599899.5:n.1142G>C
|
|
|
ENST00000601008.1:c.242-4261G>C
|
ENSP00000471384.1:n.242-4261G>C
|
|
NM_000064.3:c.4183G>C
|
NP_000055.2:p.Asp1395His
|
|
NM_000064.4:c.4183G>C
MANE Select
|
NP_000055.2:p.Asp1395His
|
|