ENST00000496887.7:c.1415G>C
|
ENSP00000434560.2:p.Arg472Pro
|
|
ENST00000646564.2:c.1232G>C
|
ENSP00000495806.2:p.Arg411Pro
|
|
ENST00000155840.12:c.1772G>C
MANE Select
|
ENSP00000155840.2:p.Arg591Pro
|
|
ENST00000335475.6:c.1391G>C
|
ENSP00000334497.5:p.Arg464Pro
|
|
ENST00000526095.2:c.176G>C
|
ENSP00000494939.1:p.Arg59Pro
|
|
ENST00000646564.1:c.878G>C
|
ENSP00000495806.1:p.Arg293Pro
|
|
ENST00000155840.9:c.1772G>C
|
ENSP00000155840.2:p.Arg591Pro
|
|
ENST00000335475.5:c.1391G>C
|
ENSP00000334497.5:p.Arg464Pro
|
|
ENST00000526095.1:n.279G>C
|
|
|
NM_000218.2:c.1772G>C , LRG_287t1:c.1772G>C
|
NP_000209.2:p.Arg591Pro
|
|
NM_181798.1:c.1391G>C , LRG_287t2:c.1391G>C
|
NP_861463.1:p.Arg464Pro
|
|
NM_000218.3:c.1772G>C
MANE Select
|
NP_000209.2:p.Arg591Pro
|
|