ENST00000455537.7:c.2953G=
MANE Select
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ENSP00000408979.2:p.Gly985=
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ENST00000674619.1:c.2974G=
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ENSP00000502270.1:p.Gly992=
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|
ENST00000675697.1:c.44G=
|
|
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ENST00000675737.1:n.357G=
|
|
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ENST00000675882.1:n.2476G=
|
|
|
ENST00000675929.1:n.1511G=
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|
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ENST00000676055.1:c.44G=
|
|
|
ENST00000676457.1:c.2848G=
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ENSP00000501588.1:p.Gly950=
|
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ENST00000286452.5:c.2686G=
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ENSP00000286452.5:p.Gly896=
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ENST00000455537.6:c.2953G=
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ENSP00000408979.2:p.Gly985=
|
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ENST00000552227.1:n.236G=
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|
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NM_004984.2:c.2953G=
|
NP_004975.2:p.Gly985=
|
|
NM_001354705.1:c.2686G=
|
NP_001341634.1:p.Gly896=
|
|
NM_004984.3:c.2953G=
|
NP_004975.2:p.Gly985=
|
|
XR_002957324.1:n.3186G=
|
|
|
NM_004984.4:c.2953G=
MANE Select
|
NP_004975.2:p.Gly985=
|
|
NM_001354705.2:c.2686G=
|
NP_001341634.1:p.Gly896=
|
|