ENST00000336906.6:c.113G>A
MANE Select
|
ENSP00000338082.4:p.Trp38Ter
|
|
ENST00000380252.6:c.-53G>A
|
ENSP00000369602.2:n.-53G>A
|
|
ENST00000380259.7:c.1659G>A
|
ENSP00000369609.3:n.1659G>A
|
|
ENST00000642908.1:c.113G>A
|
ENSP00000495346.1:p.Trp38Ter
|
|
ENST00000647543.1:c.113G>A
|
ENSP00000496470.1:p.Trp38Ter
|
|
ENST00000336906.4:c.113G>A
|
ENSP00000338082.4:p.Trp38Ter
|
|
ENST00000380252.5:c.83G>A
|
ENSP00000369602.1:p.Trp28Ter
|
|
ENST00000380259.6:c.113G>A
|
ENSP00000369609.2:p.Trp38Ter
|
|
ENST00000444587.1:c.75G>A
|
ENSP00000488218.1:p.Met25Ile
|
|
ENST00000620888.4:c.113G>A
|
ENSP00000479637.1:p.Trp38Ter
|
|
ENST00000624109.1:c.242C>T
|
ENSP00000485458.1:p.Pro81Leu
|
|
NM_000184.2:c.113G>A
|
NP_000175.1:p.Trp38Ter
|
|
NM_000184.3:c.113G>A
MANE Select
|
NP_000175.1:p.Trp38Ter
|
|