ENST00000362072.8:c.1080T>C
MANE Select
|
ENSP00000354859.3:p.Arg360=
|
|
ENST00000346454.7:c.993T>C
|
ENSP00000278597.5:p.Arg331=
|
|
ENST00000362072.7:c.1080T>C
|
ENSP00000354859.3:p.Arg360=
|
|
ENST00000538967.5:c.1086T>C
|
ENSP00000438215.1:p.Arg362=
|
|
ENST00000542968.5:c.1080T>C
|
ENSP00000442172.1:p.Arg360=
|
|
ENST00000544518.5:c.1077T>C
|
ENSP00000441068.1:p.Arg359=
|
|
NM_000795.3:c.1080T>C
|
NP_000786.1:p.Arg360=
|
|
NM_016574.3:c.993T>C
|
NP_057658.2:p.Arg331=
|
|
XM_017017296.2:c.1080T>C
|
XP_016872785.1:p.Arg360=
|
|
NM_000795.4:c.1080T>C
MANE Select
|
NP_000786.1:p.Arg360=
|
|
NM_016574.4:c.993T>C
|
NP_057658.2:p.Arg331=
|
|