ENST00000321728.12:c.275G>T
|
ENSP00000318315.7:p.Gly92Val
|
|
ENST00000643927.1:c.275G>T
MANE Select
|
ENSP00000496129.1:p.Gly92Val
|
|
ENST00000647422.1:n.175G>T
|
|
|
ENST00000303531.11:c.275G>T
|
ENSP00000305355.7:p.Gly92Val
|
|
ENST00000321728.11:c.275G>T
|
ENSP00000318315.7:p.Gly92Val
|
|
ENST00000498739.1:c.-26-104214G>T
|
ENSP00000459227.1:n.-26-104214G>T
|
|
NM_002738.6:c.275G>T
|
NP_002729.2:p.Gly92Val
|
|
NM_212535.2:c.275G>T
|
NP_997700.1:p.Gly92Val
|
|
NM_002738.7:c.275G>T
MANE Select
|
NP_002729.2:p.Gly92Val
|
|
NM_212535.3:c.275G>T
|
NP_997700.1:p.Gly92Val
|
|