ENST00000682513.1:c.8807T>A
|
ENSP00000508201.1:p.Val2936Asp
|
|
ENST00000512123.4:c.8807T>A
MANE Select
|
ENSP00000422834.2:p.Val2936Asp
|
|
ENST00000512123.3:c.8807T>A
|
ENSP00000422834.2:p.Val2936Asp
|
|
NM_025074.6:c.8807T>A
|
NP_079350.5:p.Val2936Asp
|
|
XM_006714314.1:c.8801T>A
|
XP_006714377.1:p.Val2934Asp
|
|
XM_006714316.1:c.8579T>A
|
XP_006714379.1:p.Val2860Asp
|
|
XM_011532270.1:c.6506T>A
|
XP_011530572.1:p.Val2169Asp
|
|
XM_011532271.1:c.3695T>A
|
XP_011530573.1:p.Val1232Asp
|
|
XM_006714316.3:c.8579T>A
|
XP_006714379.1:p.Val2860Asp
|
|
NM_025074.7:c.8807T>A
MANE Select
|
NP_079350.5:p.Val2936Asp
|
|