ENST00000367408.6:n.2946G=
|
|
|
ENST00000367409.9:c.9659G=
MANE Select
|
ENSP00000356379.4:p.Trp3220=
|
|
ENST00000680265.1:c.9881G=
|
ENSP00000505384.1:p.Trp3294=
|
|
ENST00000680710.1:c.9635G=
|
ENSP00000506676.1:p.Trp3212=
|
|
ENST00000294732.11:c.4904G=
|
ENSP00000294732.7:p.Trp1635=
|
|
ENST00000367408.5:c.2654G=
|
ENSP00000356378.1:p.Trp885=
|
|
ENST00000367409.8:c.9659G=
|
ENSP00000356379.4:p.Trp3220=
|
|
ENST00000612785.1:c.3617G=
|
ENSP00000479244.1:p.Trp1206=
|
|
NM_001206846.1:c.4904G=
|
NP_001193775.1:p.Trp1635=
|
|
NM_018136.4:c.9659G=
|
NP_060606.3:p.Trp3220=
|
|
NM_018136.5:c.9659G=
MANE Select
|
NP_060606.3:p.Trp3220=
|
|
NM_001206846.2:c.4904G=
|
NP_001193775.1:p.Trp1635=
|
|