ENST00000299084.9:c.878T>A
MANE Select
|
ENSP00000299084.4:p.Leu293Gln
|
|
ENST00000299084.8:c.878T>A
|
ENSP00000299084.4:p.Leu293Gln
|
|
NM_152594.2:c.878T>A
|
NP_689807.1:p.Leu293Gln
|
|
XM_005254202.2:c.914T>A
|
XP_005254259.1:p.Leu305Gln
|
|
XM_005254203.3:c.656T>A
|
XP_005254260.1:p.Leu219Gln
|
|
XM_011521288.1:c.815T>A
|
XP_011519590.1:p.Leu272Gln
|
|
XM_011521289.1:c.815T>A
|
XP_011519591.1:p.Leu272Gln
|
|
XM_011521290.1:c.815T>A
|
XP_011519592.1:p.Leu272Gln
|
|
XM_005254202.3:c.914T>A
|
XP_005254259.1:p.Leu305Gln
|
|
XM_011521289.3:c.815T>A
|
XP_011519591.1:p.Leu272Gln
|
|
NM_152594.3:c.878T>A
MANE Select
|
NP_689807.1:p.Leu293Gln
|
|