ENST00000374479.4:c.1047C>T
MANE Select
|
ENSP00000363603.3:p.Pro349=
|
|
ENST00000374479.3:c.1047C>T
|
ENSP00000363603.3:p.Pro349=
|
|
NM_000147.4:c.1047C>T
|
NP_000138.2:p.Pro349=
|
|
XM_005245821.1:c.672C>T
|
XP_005245878.1:p.Pro224=
|
|
XM_011541167.1:c.414C>T
|
XP_011539469.1:p.Pro138=
|
|
XM_005245821.3:c.672C>T
|
XP_005245878.1:p.Pro224=
|
|
XM_011541167.3:c.414C>T
|
XP_011539469.1:p.Pro138=
|
|
XM_017000905.2:c.744C>T
|
XP_016856394.1:p.Pro248=
|
|
NM_000147.5:c.1047C>T
MANE Select
|
NP_000138.2:p.Pro349=
|
|
NR_174379.1:n.1225C>T
|
|
|
NR_174380.1:n.1274C>T
|
|
|
NR_174381.1:n.1113C>T
|
|
|
NR_174382.1:n.1510C>T
|
|
|