|
ENST00000261769.10:c.2537G>C
MANE Select
|
ENSP00000261769.4:p.Ser846Thr
|
|
|
ENST00000261769.9:c.2537G>C
|
ENSP00000261769.4:p.Ser846Thr
|
|
|
ENST00000422392.6:c.2354G>C
|
ENSP00000414946.2:p.Ser785Thr
|
|
|
ENST00000562118.1:n.755G>C
|
|
|
|
ENST00000562836.5:n.2608G>C
|
|
|
|
ENST00000566510.5:c.*1203G>C
|
ENSP00000458139.1:n.*1203G>C
|
|
|
ENST00000566612.5:c.*777G>C
|
ENSP00000454782.1:n.*777G>C
|
|
|
ENST00000611625.4:c.2600G>C
|
ENSP00000481063.1:p.Ser867Thr
|
|
|
ENST00000612417.4:c.1854-804G>C
|
ENSP00000478360.1:n.1854-804G>C
|
|
|
ENST00000621016.4:c.1866-816G>C
|
ENSP00000480664.1:n.1866-816G>C
|
|
|
NM_004360.3:c.2537G>C , LRG_301t1:c.2537G>C
|
NP_004351.1:p.Ser846Thr
|
|
|
XM_011523488.1:c.1802G>C
|
XP_011521790.1:p.Ser601Thr
|
|
|
XM_011523489.1:c.1802G>C
|
XP_011521791.1:p.Ser601Thr
|
|
|
NM_001317184.1:c.2354G>C
|
NP_001304113.1:p.Ser785Thr
|
|
|
NM_001317185.1:c.989G>C
|
NP_001304114.1:p.Ser330Thr
|
|
|
NM_001317186.1:c.572G>C
|
NP_001304115.1:p.Ser191Thr
|
|
|
NM_004360.4:c.2537G>C
|
NP_004351.1:p.Ser846Thr
|
|
|
NM_004360.5:c.2537G>C
MANE Select
|
NP_004351.1:p.Ser846Thr
|
|
|
NM_001317184.2:c.2354G>C
|
NP_001304113.1:p.Ser785Thr
|
|
|
NM_001317185.2:c.989G>C
|
NP_001304114.1:p.Ser330Thr
|
|
|
NM_001317186.2:c.572G>C
|
NP_001304115.1:p.Ser191Thr
|
|
