ENST00000353578.9:c.4997T>C
|
ENSP00000315873.4:p.Met1666Thr
|
|
ENST00000295550.9:c.5615T>C
MANE Select
|
ENSP00000295550.4:p.Met1872Thr
|
|
ENST00000295550.8:c.5615T>C
|
ENSP00000295550.4:p.Met1872Thr
|
|
ENST00000347401.7:c.3794T>C
|
ENSP00000315609.4:p.Met1265Thr
|
|
ENST00000353578.8:c.4997T>C
|
ENSP00000315873.4:p.Met1666Thr
|
|
ENST00000409809.5:c.4997T>C
|
ENSP00000386844.1:p.Met1666Thr
|
|
ENST00000472056.5:c.3794T>C
|
ENSP00000418285.1:p.Met1265Thr
|
|
NM_004369.3:c.5615T>C , LRG_473t1:c.5615T>C
|
NP_004360.2:p.Met1872Thr
|
|
NM_057166.4:c.3794T>C
|
NP_476507.3:p.Met1265Thr
|
|
NM_057167.3:c.4997T>C
|
NP_476508.2:p.Met1666Thr
|
|
XM_005246065.1:c.5015T>C
|
XP_005246122.1:p.Met1672Thr
|
|
XM_005246066.1:c.4394T>C
|
XP_005246123.1:p.Met1465Thr
|
|
XM_006712253.1:c.5114T>C
|
XP_006712316.1:p.Met1705Thr
|
|
XM_011510574.1:c.5612T>C
|
XP_011508876.1:p.Met1871Thr
|
|
XM_011510575.1:c.3209T>C
|
XP_011508877.1:p.Met1070Thr
|
|
XM_017003304.1:c.3209T>C
|
XP_016858793.1:p.Met1070Thr
|
|
XM_024452684.1:c.4394T>C
|
XP_024308452.1:p.Met1465Thr
|
|
NM_004369.4:c.5615T>C
MANE Select
|
NP_004360.2:p.Met1872Thr
|
|
NM_057166.5:c.3794T>C
|
NP_476507.3:p.Met1265Thr
|
|
NM_057167.4:c.4997T>C
|
NP_476508.2:p.Met1666Thr
|
|