ENST00000376199.7:c.878T>C
|
ENSP00000365372.2:p.Met293Thr
|
|
ENST00000376207.10:c.983T>C
MANE Select
|
ENSP00000365380.4:p.Met328Thr
|
|
ENST00000455775.7:c.1052T>C
|
ENSP00000396415.3:p.Met351Thr
|
|
ENST00000518685.6:c.902T>C
|
ENSP00000428952.2:p.Met301Thr
|
|
ENST00000557224.6:c.878T>C
|
ENSP00000451208.1:p.Met293Thr
|
|
ENST00000651307.1:c.967+730T>C
|
ENSP00000498454.1:n.967+730T>C
|
|
ENST00000376197.1:c.833T>C
|
ENSP00000365369.1:p.Met278Thr
|
|
ENST00000376199.6:c.878T>C
|
ENSP00000365372.2:p.Met293Thr
|
|
ENST00000376207.8:c.983T>C
|
ENSP00000365380.4:p.Met328Thr
|
|
ENST00000455775.6:c.1052T>C
|
ENSP00000396415.3:p.Met351Thr
|
|
ENST00000518685.5:c.878T>C
|
ENSP00000428952.1:p.Met293Thr
|
|
ENST00000557224.5:c.878T>C
|
ENSP00000451208.1:p.Met293Thr
|
|
NM_001114377.1:c.878T>C
|
NP_001107849.1:p.Met293Thr
|
|
NM_014009.3:c.983T>C , LRG_62t1:c.983T>C
|
NP_054728.2:p.Met328Thr
|
|
XM_006724533.2:c.1052T>C
|
XP_006724596.2:p.Met351Thr
|
|
XM_011543915.1:c.1202T>C
|
XP_011542217.1:p.Met401Thr
|
|
XM_011543916.1:c.1202T>C
|
XP_011542218.1:p.Met401Thr
|
|
XM_011543917.1:c.1001T>C
|
XP_011542219.1:p.Met334Thr
|
|
XM_011543918.1:c.1238T>C
|
XP_011542220.1:p.Met413Thr
|
|
XM_011543919.1:c.1202T>C
|
XP_011542221.1:p.Met401Thr
|
|
XM_017029567.1:c.929T>C
|
XP_016885056.1:p.Met310Thr
|
|
NM_001114377.2:c.878T>C
|
NP_001107849.1:p.Met293Thr
|
|
NM_014009.4:c.983T>C
MANE Select
|
NP_054728.2:p.Met328Thr
|
|