ENST00000299084.9:c.635T>A
MANE Select
|
ENSP00000299084.4:p.Val212Glu
|
|
ENST00000299084.8:c.635T>A
|
ENSP00000299084.4:p.Val212Glu
|
|
NM_152594.2:c.635T>A
|
NP_689807.1:p.Val212Glu
|
|
XM_005254202.2:c.671T>A
|
XP_005254259.1:p.Val224Glu
|
|
XM_005254203.3:c.413T>A
|
XP_005254260.1:p.Val138Glu
|
|
XM_011521288.1:c.572T>A
|
XP_011519590.1:p.Val191Glu
|
|
XM_011521289.1:c.572T>A
|
XP_011519591.1:p.Val191Glu
|
|
XM_011521290.1:c.572T>A
|
XP_011519592.1:p.Val191Glu
|
|
XM_005254202.3:c.671T>A
|
XP_005254259.1:p.Val224Glu
|
|
XM_011521289.3:c.572T>A
|
XP_011519591.1:p.Val191Glu
|
|
NM_152594.3:c.635T>A
MANE Select
|
NP_689807.1:p.Val212Glu
|
|