ENST00000281928.9:c.3165G>T
MANE Select
|
ENSP00000281928.3:p.Arg1055Ser
|
|
ENST00000548743.2:c.3135G>T
|
ENSP00000448553.2:p.Arg1045Ser
|
|
ENST00000549786.2:c.2593G>T
|
|
|
ENST00000648173.1:n.1960G>T
|
|
|
ENST00000648379.1:n.1533G>T
|
|
|
ENST00000648737.1:n.2929G>T
|
|
|
ENST00000648916.1:n.1176G>T
|
|
|
ENST00000649607.1:c.1349G>T
|
|
|
ENST00000650226.1:c.3165G>T
|
ENSP00000496981.1:p.Arg1055Ser
|
|
ENST00000281928.7:c.3165G>T
|
ENSP00000281928.3:p.Arg1055Ser
|
|
NM_015335.4:c.3165G>T
|
NP_056150.1:p.Arg1055Ser
|
|
XM_011538080.1:c.3165G>T
|
XP_011536382.1:p.Arg1055Ser
|
|
XM_011538081.1:c.3162G>T
|
XP_011536383.1:p.Arg1054Ser
|
|
XM_011538082.1:c.3135G>T
|
XP_011536384.1:p.Arg1045Ser
|
|
XM_011538080.2:c.3165G>T
|
XP_011536382.1:p.Arg1055Ser
|
|
XM_011538081.2:c.3162G>T
|
XP_011536383.1:p.Arg1054Ser
|
|
XM_011538082.2:c.3135G>T
|
XP_011536384.1:p.Arg1045Ser
|
|
XM_017019090.1:c.3162G>T
|
XP_016874579.1:p.Arg1054Ser
|
|
NM_015335.5:c.3165G>T
MANE Select
|
NP_056150.1:p.Arg1055Ser
|
|