ENST00000455537.7:c.726T>A
MANE Select
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ENSP00000408979.2:p.Thr242=
|
|
ENST00000674619.1:c.726T>A
|
ENSP00000502270.1:p.Thr242=
|
|
ENST00000676457.1:c.621T>A
|
ENSP00000501588.1:p.Thr207=
|
|
ENST00000286452.5:c.459T>A
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ENSP00000286452.5:p.Thr153=
|
|
ENST00000455537.6:c.726T>A
|
ENSP00000408979.2:p.Thr242=
|
|
NM_004984.2:c.726T>A
|
NP_004975.2:p.Thr242=
|
|
NM_001354705.1:c.459T>A
|
NP_001341634.1:p.Thr153=
|
|
NM_004984.3:c.726T>A
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NP_004975.2:p.Thr242=
|
|
XR_002957324.1:n.959T>A
|
|
|
NM_004984.4:c.726T>A
MANE Select
|
NP_004975.2:p.Thr242=
|
|
NM_001354705.2:c.459T>A
|
NP_001341634.1:p.Thr153=
|
|