ENST00000357685.11:c.527A>G
MANE Select
|
ENSP00000350314.5:p.Asp176Gly
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ENST00000357685.9:c.527A>G
|
ENSP00000350314.5:p.Asp176Gly
|
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ENST00000361053.8:c.517+191A>G
|
ENSP00000354338.4:n.517+191A>G
|
|
ENST00000438022.5:c.425A>G
|
ENSP00000414843.1:p.Asp142Gly
|
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ENST00000460924.6:n.800A>G
|
|
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ENST00000494860.5:n.560A>G
|
|
|
ENST00000526088.5:c.425A>G
|
ENSP00000436615.1:p.Asp142Gly
|
|
ENST00000527939.1:c.*169A>G
|
ENSP00000436956.1:n.*169A>G
|
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ENST00000530677.1:c.222A>G
|
|
|
ENST00000531169.5:c.425A>G
|
ENSP00000437053.1:p.Asp142Gly
|
|
ENST00000532593.5:c.212A>G
|
ENSP00000431802.1:p.Asp71Gly
|
|
ENST00000532612.5:c.447+191A>G
|
|
|
ENST00000534550.5:c.*159+191A>G
|
ENSP00000434488.1:n.*159+191A>G
|
|
NM_001037290.2:c.425A>G
|
NP_001032367.2:p.Asp142Gly
|
|
NM_001256397.1:c.425A>G
|
NP_001243326.1:p.Asp142Gly
|
|
NM_001256398.1:c.517+191A>G
|
NP_001243327.1:n.517+191A>G
|
|
NM_001256400.1:c.212A>G
|
NP_001243329.1:p.Asp71Gly
|
|
NM_031938.5:c.527A>G
|
NP_114144.4:p.Asp176Gly
|
|
NM_001037290.3:c.425A>G
|
NP_001032367.3:p.Asp142Gly
|
|
NM_001256397.2:c.425A>G
|
NP_001243326.2:p.Asp142Gly
|
|
NM_001256398.2:c.517+191A>G
|
NP_001243327.2:n.517+191A>G
|
|
NM_001256400.2:c.212A>G
|
NP_001243329.2:p.Asp71Gly
|
|
NM_031938.7:c.527A>G
MANE Select
|
NP_114144.5:p.Asp176Gly
|
|
NM_001037290.4:c.425A>G
|
NP_001032367.3:p.Asp142Gly
|
|
NM_001256397.3:c.425A>G
|
NP_001243326.2:p.Asp142Gly
|
|
NM_001256398.3:c.517+191A>G
|
NP_001243327.2:n.517+191A>G
|
|
NM_001256400.3:c.212A>G
|
NP_001243329.2:p.Asp71Gly
|
|