ENST00000236671.7:c.1091C>G
MANE Select
|
ENSP00000236671.2:p.Thr364Ser
|
|
ENST00000367196.4:c.986C>G
|
ENSP00000356164.4:p.Thr329Ser
|
|
ENST00000427721.3:c.516C>G
|
|
|
ENST00000429746.2:c.986C>G
|
ENSP00000402586.2:p.Thr329Ser
|
|
ENST00000433655.6:c.*257C>G
|
ENSP00000404902.1:n.*257C>G
|
|
ENST00000438213.6:c.1208C>G
|
ENSP00000415036.2:p.Thr403Ser
|
|
ENST00000636397.1:c.1071+152C>G
|
ENSP00000489910.1:n.1071+152C>G
|
|
ENST00000636571.1:c.1070C>G
|
ENSP00000490770.1:p.Thr357Ser
|
|
ENST00000636579.1:c.72+152C>G
|
ENSP00000490489.1:n.72+152C>G
|
|
ENST00000636615.1:c.1071+152C>G
|
ENSP00000490014.1:n.1071+152C>G
|
|
ENST00000636843.1:c.1085C>G
|
ENSP00000490897.1:p.Thr362Ser
|
|
ENST00000637158.1:n.689C>G
|
|
|
ENST00000637381.2:n.3519C>G
|
|
|
ENST00000637387.1:c.1070C>G
|
ENSP00000490598.1:p.Thr357Ser
|
|
ENST00000637815.2:c.1073C>G
|
ENSP00000490344.1:p.Thr358Ser
|
|
ENST00000637915.1:c.1082C>G
|
ENSP00000490471.1:p.Thr361Ser
|
|
ENST00000637937.1:n.399C>G
|
|
|
ENST00000678991.1:c.*952C>G
|
ENSP00000503019.1:n.*952C>G
|
|
ENST00000236671.6:c.1091C>G
|
ENSP00000236671.2:p.Thr364Ser
|
|
ENST00000427721.2:c.471+152C>G
|
ENSP00000415840.2:n.471+152C>G
|
|
ENST00000429746.1:c.422C>G
|
ENSP00000402586.1:p.Thr141Ser
|
|
ENST00000433655.5:c.*257C>G
|
ENSP00000404902.1:n.*257C>G
|
|
NM_001909.4:c.1091C>G
|
NP_001900.1:p.Thr364Ser
|
|
NM_001909.5:c.1091C>G
MANE Select
|
NP_001900.1:p.Thr364Ser
|
|