ENST00000367435.5:c.632G>C
MANE Select
|
ENSP00000356405.4:p.Arg211Thr
|
|
ENST00000635846.1:c.632G>C
|
ENSP00000490035.1:p.Arg211Thr
|
|
ENST00000643006.1:c.632G>C
|
ENSP00000496633.1:p.Arg211Thr
|
|
ENST00000643784.1:c.*108G>C
|
ENSP00000494944.1:n.*108G>C
|
|
ENST00000647662.1:n.533G>C
|
|
|
ENST00000648071.1:c.*608G>C
|
ENSP00000497513.1:n.*608G>C
|
|
ENST00000649606.1:n.645G>C
|
|
|
ENST00000649895.1:n.850G>C
|
|
|
ENST00000650197.1:c.632G>C
|
ENSP00000496929.1:p.Arg211Thr
|
|
ENST00000367435.3:c.632G>C
|
ENSP00000356405.3:p.Arg211Thr
|
|
NM_024529.4:c.632G>C , LRG_507t1:c.632G>C
|
NP_078805.3:p.Arg211Thr
|
|
XM_006711537.2:c.632G>C
|
XP_006711600.1:p.Arg211Thr
|
|
XM_006711537.4:c.632G>C
|
XP_006711600.1:p.Arg211Thr
|
|
NM_024529.5:c.632G>C
MANE Select
|
NP_078805.3:p.Arg211Thr
|
|