ENST00000330684.4:c.2828A>C
MANE Select
|
ENSP00000332549.3:p.Tyr943Ser
|
|
ENST00000535259.6:c.2357A>C
|
ENSP00000441572.3:p.Tyr786Ser
|
|
ENST00000636273.2:n.2421A>C
|
|
|
ENST00000674742.1:c.2357A>C
|
ENSP00000502200.1:p.Tyr786Ser
|
|
ENST00000675398.1:c.*198A>C
|
ENSP00000502752.1:n.*198A>C
|
|
ENST00000330684.3:c.2828A>C
|
ENSP00000332549.3:p.Tyr943Ser
|
|
ENST00000396573.6:c.2828A>C
|
ENSP00000379818.2:p.Tyr943Ser
|
|
ENST00000396575.6:c.2417A>C
|
ENSP00000379820.3:p.Tyr806Ser
|
|
ENST00000461292.3:n.2467A>C
|
|
|
ENST00000535259.5:c.2417A>C
|
ENSP00000441572.2:p.Tyr806Ser
|
|
ENST00000562109.5:c.2828A>C
|
ENSP00000454998.1:p.Tyr943Ser
|
|
NM_000833.4:c.2828A>C
|
NP_000824.1:p.Tyr943Ser
|
|
NM_001134407.2:c.2828A>C
|
NP_001127879.1:p.Tyr943Ser
|
|
NM_001134408.2:c.2828A>C
|
NP_001127880.1:p.Tyr943Ser
|
|
XM_011522456.1:c.2669A>C
|
XP_011520758.1:p.Tyr890Ser
|
|
XM_011522457.1:c.2570A>C
|
XP_011520759.1:p.Tyr857Ser
|
|
XM_011522458.1:c.2357A>C
|
XP_011520760.1:p.Tyr786Ser
|
|
XM_011522459.1:c.2357A>C
|
XP_011520761.1:p.Tyr786Ser
|
|
XM_011522460.1:c.2357A>C
|
XP_011520762.1:p.Tyr786Ser
|
|
XM_011522461.1:c.2828A>C
|
XP_011520763.1:p.Tyr943Ser
|
|
XM_011522458.3:c.2357A>C
|
XP_011520760.1:p.Tyr786Ser
|
|
XM_011522461.3:c.2828A>C
|
XP_011520763.1:p.Tyr943Ser
|
|
XM_017023172.1:c.2984A>C
|
XP_016878661.1:p.Tyr995Ser
|
|
XM_017023173.1:c.2984A>C
|
XP_016878662.1:p.Tyr995Ser
|
|
NM_001134407.3:c.2828A>C
MANE Select
|
NP_001127879.1:p.Tyr943Ser
|
|
NM_000833.5:c.2828A>C
|
NP_000824.1:p.Tyr943Ser
|
|