ENST00000431168.2:c.229G=
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ENSP00000393455.2:p.Gly77=
|
|
ENST00000292327.6:c.229G=
MANE Select
|
ENSP00000292327.4:p.Gly77=
|
|
ENST00000653454.1:c.229G=
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ENSP00000499624.1:p.Gly77=
|
|
ENST00000654597.1:c.229G=
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ENSP00000499406.1:p.Gly77=
|
|
ENST00000655244.1:n.451G=
|
|
|
ENST00000662933.1:c.229G=
|
ENSP00000499577.1:p.Gly77=
|
|
ENST00000664891.1:n.187G=
|
|
|
ENST00000292327.4:c.229G=
|
ENSP00000292327.4:p.Gly77=
|
|
ENST00000395869.5:c.229G=
|
ENSP00000379210.1:p.Gly77=
|
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NM_000258.2:c.229G= , LRG_395t1:c.229G=
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NP_000249.1:p.Gly77=
|
|
NM_000258.3:c.229G=
MANE Select
|
NP_000249.1:p.Gly77=
|
|