ENST00000376883.2:c.1539A>T
MANE Select
|
ENSP00000366080.2:p.Arg513Ser
|
|
ENST00000488757.6:c.1323A>T
|
ENSP00000418259.2:p.Arg441Ser
|
|
ENST00000376881.4:c.1287A>T
|
ENSP00000366078.4:p.Arg429Ser
|
|
ENST00000376883.1:c.1479A>T
|
ENSP00000366080.1:p.Arg493Ser
|
|
ENST00000488757.5:c.1539A>T
|
ENSP00000418259.1:p.Arg513Ser
|
|
NM_001109809.2:c.1539A>T
|
NP_001103279.2:p.Arg513Ser
|
|
XM_006715087.2:c.1323A>T
|
XP_006715150.1:p.Arg441Ser
|
|
XM_011514570.1:c.1539A>T
|
XP_011512872.1:p.Arg513Ser
|
|
NM_001109809.3:c.1539A>T
|
NP_001103279.2:p.Arg513Ser
|
|
NM_001366333.1:c.1323A>T
|
NP_001353262.1:p.Arg441Ser
|
|
NM_001109809.4:c.1539A>T
|
NP_001103279.2:p.Arg513Ser
|
|
NM_001366333.2:c.1323A>T
|
NP_001353262.1:p.Arg441Ser
|
|
NM_001109809.5:c.1539A>T
MANE Select
|
NP_001103279.2:p.Arg513Ser
|
|