ENST00000559133.6:c.5550T>C
|
ENSP00000453958.2:p.Arg1850=
|
|
ENST00000674301.2:c.5550T>C
|
ENSP00000501333.2:p.Arg1850=
|
|
ENST00000684448.1:n.4224T>C
|
|
|
ENST00000316623.10:c.5550T>C
MANE Select
|
ENSP00000325527.5:p.Arg1850=
|
|
ENST00000674301.1:c.549T>C
|
ENSP00000501333.1:p.Arg183=
|
|
ENST00000316623.9:c.5550T>C
|
ENSP00000325527.5:p.Arg1850=
|
|
ENST00000537463.6:c.*1313T>C
|
ENSP00000440294.2:n.*1313T>C
|
|
ENST00000559133.5:c.857T>C
|
|
|
NM_000138.4:c.5550T>C , LRG_778t1:c.5550T>C
|
NP_000129.3:p.Arg1850=
|
|
NM_000138.5:c.5550T>C
MANE Select
|
NP_000129.3:p.Arg1850=
|
|