ENST00000641284.2:c.107G>C
|
ENSP00000493088.1:p.Trp36Ser
|
|
ENST00000646677.2:c.107G>C
|
ENSP00000496533.1:p.Trp36Ser
|
|
ENST00000641284.1:c.107G>C
|
ENSP00000493088.1:p.Trp36Ser
|
|
ENST00000646677.1:c.107G>C
|
ENSP00000496533.1:p.Trp36Ser
|
|
ENST00000647318.2:c.107G>C
MANE Select
|
ENSP00000495993.1:p.Trp36Ser
|
|
ENST00000300589.6:c.188G>C
|
ENSP00000300589.2:p.Trp63Ser
|
|
ENST00000526417.6:n.175G>C
|
|
|
ENST00000527070.5:c.*803G>C
|
ENSP00000435149.1:n.*803G>C
|
|
ENST00000531674.1:c.107G>C
|
ENSP00000431681.1:p.Trp36Ser
|
|
ENST00000532206.1:n.292G>C
|
|
|
NM_001293557.1:c.107G>C
|
NP_001280486.1:p.Trp36Ser
|
|
NM_022162.2:c.188G>C
|
NP_071445.1:p.Trp63Ser
|
|
XM_005256084.2:c.107G>C
|
XP_005256141.1:p.Trp36Ser
|
|
XM_006721242.2:c.107G>C
|
XP_006721305.1:p.Trp36Ser
|
|
XM_006721243.2:c.107G>C
|
XP_006721306.1:p.Trp36Ser
|
|
XM_011523258.1:c.-38+5940G>C
|
XP_011521560.1:n.-38+5940G>C
|
|
XM_011523259.1:c.-373G>C
|
XP_011521561.1:n.-373G>C
|
|
XM_011523260.1:c.107G>C
|
XP_011521562.1:p.Trp36Ser
|
|
XM_011523261.1:c.107G>C
|
XP_011521563.1:p.Trp36Ser
|
|
XR_429725.2:n.197G>C
|
|
|
XR_429726.2:n.197G>C
|
|
|
XR_933387.1:n.197G>C
|
|
|
XM_005256084.4:c.107G>C
|
XP_005256141.1:p.Trp36Ser
|
|
XM_006721242.4:c.107G>C
|
XP_006721305.1:p.Trp36Ser
|
|
XM_006721243.4:c.107G>C
|
XP_006721306.1:p.Trp36Ser
|
|
XM_011523259.2:c.-373G>C
|
XP_011521561.1:n.-373G>C
|
|
XM_011523260.3:c.107G>C
|
XP_011521562.1:p.Trp36Ser
|
|
XM_011523261.2:c.107G>C
|
XP_011521563.1:p.Trp36Ser
|
|
XM_017023536.1:c.-127+5940G>C
|
XP_016879025.1:n.-127+5940G>C
|
|
XM_017023537.1:c.-21+5940G>C
|
XP_016879026.1:n.-21+5940G>C
|
|
XR_429725.3:n.150G>C
|
|
|
XR_429726.3:n.150G>C
|
|
|
XR_933387.2:n.150G>C
|
|
|
NM_001293557.2:c.107G>C
|
NP_001280486.1:p.Trp36Ser
|
|
NM_001370466.1:c.107G>C
MANE Select
|
NP_001357395.1:p.Trp36Ser
|
|
NM_022162.3:c.188G>C
|
NP_071445.1:p.Trp63Ser
|
|
NR_163434.1:n.172G>C
|
|
|