ENST00000313601.11:c.547A>T
MANE Select
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ENSP00000312999.6:p.Thr183Ser
|
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ENST00000266027.9:c.391A>T
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ENSP00000266027.6:p.Thr131Ser
|
|
ENST00000313601.10:c.547A>T
|
ENSP00000312999.6:p.Thr183Ser
|
|
ENST00000422163.5:c.499A>T
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ENSP00000406871.1:p.Thr167Ser
|
|
ENST00000440628.5:c.391A>T
|
ENSP00000395736.1:p.Thr131Ser
|
|
ENST00000441156.5:c.*75A>T
|
ENSP00000394321.1:n.*75A>T
|
|
ENST00000446079.5:c.*182A>T
|
ENSP00000406065.1:n.*182A>T
|
|
ENST00000451956.1:c.436A>T
|
ENSP00000406369.1:p.Thr146Ser
|
|
ENST00000468422.1:n.114A>T
|
|
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ENST00000490122.5:n.1374A>T
|
|
|
ENST00000491100.5:n.2363A>T
|
|
|
NM_001166425.1:c.436A>T
|
NP_001159897.1:p.Thr146Ser
|
|
NM_001282617.1:c.391A>T
|
NP_001269546.1:p.Thr131Ser
|
|
NM_001282618.1:c.304A>T
|
NP_001269547.1:p.Thr102Ser
|
|
NM_001282619.1:c.499A>T
|
NP_001269548.1:p.Thr167Ser
|
|
NM_001282620.1:c.499A>T
|
NP_001269549.1:p.Thr167Ser
|
|
NM_002070.3:c.547A>T
|
NP_002061.1:p.Thr183Ser
|
|
NM_002070.4:c.547A>T
MANE Select
|
NP_002061.1:p.Thr183Ser
|
|
NM_001166425.2:c.436A>T
|
NP_001159897.1:p.Thr146Ser
|
|
NM_001282618.2:c.304A>T
|
NP_001269547.1:p.Thr102Ser
|
|
NM_001282619.2:c.499A>T
|
NP_001269548.1:p.Thr167Ser
|
|
NM_001282620.2:c.499A>T
|
NP_001269549.1:p.Thr167Ser
|
|
NM_001282617.2:c.391A>T
|
NP_001269546.1:p.Thr131Ser
|
|