ENST00000382276.8:c.707C>T
MANE Select
|
ENSP00000371711.3:p.Ala236Val
|
|
ENST00000382276.7:c.707C>T
|
ENSP00000371711.3:p.Ala236Val
|
|
ENST00000564322.1:n.856C>T
|
|
|
ENST00000569227.1:c.233C>T
|
ENSP00000454701.1:p.Ala78Val
|
|
NM_021951.2:c.707C>T
|
NP_068770.2:p.Ala236Val
|
|
XM_006716732.1:c.707C>T
|
XP_006716795.1:p.Ala236Val
|
|
XM_011517770.1:c.755C>T
|
XP_011516072.1:p.Ala252Val
|
|
XM_011517771.1:c.755C>T
|
XP_011516073.1:p.Ala252Val
|
|
XM_011517772.1:c.755C>T
|
XP_011516074.1:p.Ala252Val
|
|
XM_011517773.1:c.233C>T
|
XP_011516075.1:p.Ala78Val
|
|
NM_001363767.1:c.233C>T
|
NP_001350696.1:p.Ala78Val
|
|
XM_011517773.3:c.233C>T
|
XP_011516075.1:p.Ala78Val
|
|
XM_017014374.1:c.587-22683C>T
|
XP_016869863.1:n.587-22683C>T
|
|
XM_017014375.1:c.539-22683C>T
|
XP_016869864.1:n.539-22683C>T
|
|
XM_024447434.1:c.161C>T
|
XP_024303202.1:p.Ala54Val
|
|
NM_021951.3:c.707C>T
MANE Select
|
NP_068770.2:p.Ala236Val
|
|