ENST00000374479.4:c.1158A>C
MANE Select
|
ENSP00000363603.3:p.Val386=
|
|
ENST00000374479.3:c.1158A>C
|
ENSP00000363603.3:p.Val386=
|
|
NM_000147.4:c.1158A>C
|
NP_000138.2:p.Val386=
|
|
XM_005245821.1:c.783A>C
|
XP_005245878.1:p.Val261=
|
|
XM_011541167.1:c.525A>C
|
XP_011539469.1:p.Val175=
|
|
XM_005245821.3:c.783A>C
|
XP_005245878.1:p.Val261=
|
|
XM_011541167.3:c.525A>C
|
XP_011539469.1:p.Val175=
|
|
XM_017000905.2:c.855A>C
|
XP_016856394.1:p.Val285=
|
|
NM_000147.5:c.1158A>C
MANE Select
|
NP_000138.2:p.Val386=
|
|
NR_174379.1:n.1336A>C
|
|
|
NR_174380.1:n.1385A>C
|
|
|
NR_174381.1:n.1224A>C
|
|
|
NR_174382.1:n.1621A>C
|
|
|