ENST00000374479.4:c.1032T=
MANE Select
|
ENSP00000363603.3:p.Asp344=
|
|
ENST00000374479.3:c.1032T=
|
ENSP00000363603.3:p.Asp344=
|
|
NM_000147.4:c.1032T=
|
NP_000138.2:p.Asp344=
|
|
XM_005245821.1:c.657T=
|
XP_005245878.1:p.Asp219=
|
|
XM_011541167.1:c.399T=
|
XP_011539469.1:p.Asp133=
|
|
XM_005245821.3:c.657T=
|
XP_005245878.1:p.Asp219=
|
|
XM_011541167.3:c.399T=
|
XP_011539469.1:p.Asp133=
|
|
XM_017000905.2:c.729T=
|
XP_016856394.1:p.Asp243=
|
|
NM_000147.5:c.1032T=
MANE Select
|
NP_000138.2:p.Asp344=
|
|
NR_174379.1:n.1210T=
|
|
|
NR_174380.1:n.1259T=
|
|
|
NR_174381.1:n.1098T=
|
|
|
NR_174382.1:n.1495T=
|
|
|