ENST00000322776.11:c.574G>T
MANE Select
|
ENSP00000322450.6:p.Asp192Tyr
|
|
ENST00000647561.1:c.574G>T
|
ENSP00000497587.1:p.Asp192Tyr
|
|
ENST00000322776.10:c.574G>T
|
ENSP00000322450.6:p.Asp192Tyr
|
|
ENST00000415352.6:c.553G>T
|
ENSP00000395368.2:p.Asp185Tyr
|
|
ENST00000526169.1:n.316G>T
|
|
|
ENST00000526770.5:n.433G>T
|
|
|
ENST00000529927.5:c.547G>T
|
ENSP00000436766.1:p.Asp183Tyr
|
|
ENST00000532244.5:c.271G>T
|
ENSP00000435202.1:p.Asp91Tyr
|
|
ENST00000532303.5:c.271G>T
|
ENSP00000432015.1:p.Asp91Tyr
|
|
ENST00000532343.5:c.271G>T
|
ENSP00000431751.1:p.Asp91Tyr
|
|
ENST00000533919.5:c.52G>T
|
ENSP00000435199.1:p.Asp18Tyr
|
|
NM_001166102.1:c.547G>T
|
NP_001159574.1:p.Asp183Tyr
|
|
NM_007103.3:c.574G>T
|
NP_009034.2:p.Asp192Tyr
|
|
NM_001166102.2:c.547G>T
|
NP_001159574.1:p.Asp183Tyr
|
|
NM_007103.4:c.574G>T
MANE Select
|
NP_009034.2:p.Asp192Tyr
|
|