ENST00000372409.8:c.1857C>T
MANE Select
|
ENSP00000361486.3:p.Arg619=
|
|
ENST00000372409.7:c.1857C>T
|
ENSP00000361486.3:p.Arg619=
|
|
ENST00000479348.2:c.713C>T
|
|
|
NM_022104.3:c.1857C>T
|
NP_071387.1:p.Arg619=
|
|
XM_011528980.1:c.1857C>T
|
XP_011527282.1:p.Arg619=
|
|
XM_011528981.1:c.1857C>T
|
XP_011527283.1:p.Arg619=
|
|
XM_011528982.1:c.813C>T
|
XP_011527284.1:p.Arg271=
|
|
XM_011528980.3:c.1857C>T
|
XP_011527282.1:p.Arg619=
|
|
XM_011528981.3:c.1857C>T
|
XP_011527283.1:p.Arg619=
|
|
XM_017028013.2:c.1857C>T
|
XP_016883502.1:p.Arg619=
|
|
XM_017028014.2:c.813C>T
|
XP_016883503.1:p.Arg271=
|
|
NM_022104.4:c.1857C>T
MANE Select
|
NP_071387.1:p.Arg619=
|
|