ENST00000242317.9:c.1899C=
MANE Select
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ENSP00000242317.4:p.Thr633=
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ENST00000242317.8:c.1899C=
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ENSP00000242317.4:p.Thr633=
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ENST00000442556.1:c.329+2626C=
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ENST00000470169.5:c.687C=
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ENST00000485580.1:n.475C=
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ENST00000614641.4:c.1911C=
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ENSP00000480538.1:p.Thr637=
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NM_001281428.1:c.1911C=
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NP_001268357.1:p.Thr637=
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NM_012144.3:c.1899C=
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NP_036276.1:p.Thr633=
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XM_006716758.2:c.1368C=
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XP_006716821.1:p.Thr456=
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XM_011517848.1:c.1653C=
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XP_011516150.1:p.Thr551=
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XM_006716758.3:c.1368C=
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XP_006716821.1:p.Thr456=
|
|
XM_011517848.2:c.1653C=
|
XP_011516150.1:p.Thr551=
|
|
XM_017014625.2:c.1641C=
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XP_016870114.1:p.Thr547=
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XR_002956774.1:n.2002C=
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|
|
NM_012144.4:c.1899C=
MANE Select
|
NP_036276.1:p.Thr633=
|
|
NM_001281428.2:c.1911C=
|
NP_001268357.1:p.Thr637=
|
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