ENST00000227451.4:c.1026G>A
MANE Select
|
ENSP00000227451.3:p.Ala342=
|
|
ENST00000227451.3:c.1026G>A
|
ENSP00000227451.3:p.Ala342=
|
|
ENST00000531902.1:n.145G>A
|
|
|
ENST00000532982.5:c.708G>A
|
ENSP00000434055.1:p.Ala236=
|
|
NM_001300727.1:c.708G>A
|
NP_001287656.1:p.Ala236=
|
|
NM_015177.1:c.1026G>A
|
NP_055992.1:p.Ala342=
|
|
XM_006718483.2:c.708G>A
|
XP_006718546.1:p.Ala236=
|
|
XM_006718483.3:c.708G>A
|
XP_006718546.1:p.Ala236=
|
|
NM_015177.2:c.1026G>A
MANE Select
|
NP_055992.1:p.Ala342=
|
|
NM_001300727.2:c.708G>A
|
NP_001287656.1:p.Ala236=
|
|