ENST00000299314.12:c.2850G>T
MANE Select
|
ENSP00000299314.7:p.Ser950=
|
|
ENST00000299314.11:c.2850G>T
|
ENSP00000299314.7:p.Ser950=
|
|
NM_024312.4:c.2850G>T
|
NP_077288.2:p.Ser950=
|
|
XM_006719593.2:c.2850G>T
|
XP_006719656.1:p.Ser950=
|
|
XM_011538731.1:c.2769G>T
|
XP_011537033.1:p.Ser923=
|
|
XM_006719593.3:c.2850G>T
|
XP_006719656.1:p.Ser950=
|
|
XM_011538731.2:c.2769G>T
|
XP_011537033.1:p.Ser923=
|
|
XM_017019961.1:c.2634G>T
|
XP_016875450.1:p.Ser878=
|
|
XM_017019962.2:c.1623G>T
|
XP_016875451.1:p.Ser541=
|
|
NM_024312.5:c.2850G>T
MANE Select
|
NP_077288.2:p.Ser950=
|
|