ENST00000559133.6:c.6729G=
|
ENSP00000453958.2:p.Arg2243=
|
|
ENST00000674301.2:c.*180G=
|
ENSP00000501333.2:n.*180G=
|
|
ENST00000682170.1:n.338G=
|
|
|
ENST00000316623.10:c.6729G=
MANE Select
|
ENSP00000325527.5:p.Arg2243=
|
|
ENST00000674301.1:c.1833G=
|
ENSP00000501333.1:n.1833G=
|
|
ENST00000316623.9:c.6729G=
|
ENSP00000325527.5:p.Arg2243=
|
|
ENST00000537463.6:c.*2492G=
|
ENSP00000440294.2:n.*2492G=
|
|
ENST00000559133.5:c.2036G=
|
|
|
ENST00000560720.1:n.16G=
|
|
|
NM_000138.4:c.6729G= , LRG_778t1:c.6729G=
|
NP_000129.3:p.Arg2243=
|
|
NM_000138.5:c.6729G=
MANE Select
|
NP_000129.3:p.Arg2243=
|
|