ENST00000367408.6:n.2761G>A
|
|
|
ENST00000367409.9:c.9474G>A
MANE Select
|
ENSP00000356379.4:p.Lys3158=
|
|
ENST00000680265.1:c.9696G>A
|
ENSP00000505384.1:p.Lys3232=
|
|
ENST00000680710.1:c.9450G>A
|
ENSP00000506676.1:p.Lys3150=
|
|
ENST00000294732.11:c.4719G>A
|
ENSP00000294732.7:p.Lys1573=
|
|
ENST00000367408.5:c.2469G>A
|
ENSP00000356378.1:p.Lys823=
|
|
ENST00000367409.8:c.9474G>A
|
ENSP00000356379.4:p.Lys3158=
|
|
ENST00000612785.1:c.3432G>A
|
ENSP00000479244.1:p.Lys1144=
|
|
NM_001206846.1:c.4719G>A
|
NP_001193775.1:p.Lys1573=
|
|
NM_018136.4:c.9474G>A
|
NP_060606.3:p.Lys3158=
|
|
NM_018136.5:c.9474G>A
MANE Select
|
NP_060606.3:p.Lys3158=
|
|
NM_001206846.2:c.4719G>A
|
NP_001193775.1:p.Lys1573=
|
|