ENST00000474174.2:n.552T>C
|
|
|
ENST00000698625.1:c.1308T>C
|
ENSP00000513844.1:p.Asp436=
|
|
ENST00000698626.1:c.1308T>C
|
ENSP00000513845.1:p.Asp436=
|
|
ENST00000698635.1:c.1308T>C
|
ENSP00000513850.1:p.Asp436=
|
|
ENST00000376701.5:c.1308T>C
MANE Select
|
ENSP00000365891.4:p.Asp436=
|
|
ENST00000376701.4:c.1308T>C
|
ENSP00000365891.4:p.Asp436=
|
|
ENST00000470107.1:n.17T>C
|
|
|
NM_000377.2:c.1308T>C , LRG_125t1:c.1308T>C
|
NP_000368.1:p.Asp436=
|
|
XM_011543977.1:c.1152T>C
|
XP_011542279.1:p.Asp384=
|
|
XM_011543977.2:c.1152T>C
|
XP_011542279.1:p.Asp384=
|
|
XM_017029786.1:c.1308T>C
|
XP_016885275.1:p.Asp436=
|
|
NM_000377.3:c.1308T>C
MANE Select
|
NP_000368.1:p.Asp436=
|
|