ENST00000236671.7:c.1041C>G
MANE Select
|
ENSP00000236671.2:p.Tyr347Ter
|
|
ENST00000367196.4:c.936C>G
|
ENSP00000356164.4:p.Tyr312Ter
|
|
ENST00000427721.3:c.466C>G
|
|
|
ENST00000429746.2:c.936C>G
|
ENSP00000402586.2:p.Tyr312Ter
|
|
ENST00000433655.6:c.*207C>G
|
ENSP00000404902.1:n.*207C>G
|
|
ENST00000438213.6:c.1158C>G
|
ENSP00000415036.2:p.Tyr386Ter
|
|
ENST00000497544.3:n.749C>G
|
|
|
ENST00000636397.1:c.1041C>G
|
ENSP00000489910.1:p.Tyr347Ter
|
|
ENST00000636571.1:c.1020C>G
|
ENSP00000490770.1:p.Tyr340Ter
|
|
ENST00000636579.1:c.42C>G
|
ENSP00000490489.1:p.Tyr14Ter
|
|
ENST00000636615.1:c.1041C>G
|
ENSP00000490014.1:p.Tyr347Ter
|
|
ENST00000636843.1:c.1035C>G
|
ENSP00000490897.1:p.Tyr345Ter
|
|
ENST00000637158.1:n.639C>G
|
|
|
ENST00000637381.2:n.3469C>G
|
|
|
ENST00000637387.1:c.1020C>G
|
ENSP00000490598.1:p.Tyr340Ter
|
|
ENST00000637815.2:c.1023C>G
|
ENSP00000490344.1:p.Tyr341Ter
|
|
ENST00000637915.1:c.1041C>G
|
ENSP00000490471.1:p.Tyr347Ter
|
|
ENST00000637937.1:n.349C>G
|
|
|
ENST00000678991.1:c.*902C>G
|
ENSP00000503019.1:n.*902C>G
|
|
ENST00000236671.6:c.1041C>G
|
ENSP00000236671.2:p.Tyr347Ter
|
|
ENST00000427721.2:c.441C>G
|
ENSP00000415840.2:p.Tyr147Ter
|
|
ENST00000429746.1:c.372C>G
|
ENSP00000402586.1:p.Tyr124Ter
|
|
ENST00000433655.5:c.*207C>G
|
ENSP00000404902.1:n.*207C>G
|
|
ENST00000497544.1:n.749C>G
|
|
|
NM_001909.4:c.1041C>G
|
NP_001900.1:p.Tyr347Ter
|
|
NM_001909.5:c.1041C>G
MANE Select
|
NP_001900.1:p.Tyr347Ter
|
|