ENST00000322776.11:c.594G>T
MANE Select
|
ENSP00000322450.6:p.Val198=
|
|
ENST00000647561.1:c.594G>T
|
ENSP00000497587.1:p.Val198=
|
|
ENST00000322776.10:c.594G>T
|
ENSP00000322450.6:p.Val198=
|
|
ENST00000415352.6:c.573G>T
|
ENSP00000395368.2:p.Val191=
|
|
ENST00000526169.1:n.336G>T
|
|
|
ENST00000526770.5:n.453G>T
|
|
|
ENST00000529927.5:c.567G>T
|
ENSP00000436766.1:p.Val189=
|
|
ENST00000532244.5:c.291G>T
|
ENSP00000435202.1:p.Val97=
|
|
ENST00000532303.5:c.291G>T
|
ENSP00000432015.1:p.Val97=
|
|
ENST00000533919.5:c.72G>T
|
ENSP00000435199.1:p.Val24=
|
|
NM_001166102.1:c.567G>T
|
NP_001159574.1:p.Val189=
|
|
NM_007103.3:c.594G>T
|
NP_009034.2:p.Val198=
|
|
NM_001166102.2:c.567G>T
|
NP_001159574.1:p.Val189=
|
|
NM_007103.4:c.594G>T
MANE Select
|
NP_009034.2:p.Val198=
|
|