ENST00000233575.7:c.747T>G
MANE Select
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ENSP00000233575.2:p.Ser249=
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ENST00000233575.6:c.747T>G
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ENSP00000233575.2:p.Ser249=
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ENST00000427123.5:c.*557T>G
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ENSP00000405399.1:n.*557T>G
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ENST00000440760.5:c.*592T>G
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ENSP00000399727.1:n.*592T>G
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ENST00000453453.1:c.*274T>G
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ENSP00000401922.1:n.*274T>G
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ENST00000493711.1:n.464T>G
|
|
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ENST00000494893.5:n.923T>G
|
|
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ENST00000537606.5:c.672T>G
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ENSP00000439208.1:p.Ser224=
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NM_001267059.1:c.711T>G
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NP_001253988.1:p.Ser237=
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NM_001267060.1:c.672T>G
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NP_001253989.1:p.Ser224=
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NM_001267061.1:c.687T>G
|
NP_001253990.1:p.Ser229=
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|
NM_014748.3:c.747T>G
|
NP_055563.1:p.Ser249=
|
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NR_049782.1:n.1120T>G
|
|
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NR_049783.1:n.1093T>G
|
|
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NR_049784.1:n.1069T>G
|
|
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NR_049785.1:n.1002T>G
|
|
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NR_049786.1:n.951T>G
|
|
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NR_049787.1:n.802T>G
|
|
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NR_049788.1:n.732T>G
|
|
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XM_011533203.1:c.105T>G
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XP_011531505.1:p.Ser35=
|
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XM_011533203.2:c.105T>G
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XP_011531505.1:p.Ser35=
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XM_017005405.2:c.105T>G
|
XP_016860894.1:p.Ser35=
|
|
NM_014748.4:c.747T>G
MANE Select
|
NP_055563.1:p.Ser249=
|
|
NM_001267059.2:c.711T>G
|
NP_001253988.1:p.Ser237=
|
|
NM_001267061.2:c.687T>G
|
NP_001253990.1:p.Ser229=
|
|
NR_049782.2:n.1000T>G
|
|
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NR_049783.2:n.973T>G
|
|
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NR_049784.2:n.949T>G
|
|
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NR_049785.2:n.882T>G
|
|
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NR_049786.2:n.831T>G
|
|
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NR_049787.2:n.682T>G
|
|
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NR_049788.2:n.612T>G
|
|
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NM_001267060.2:c.672T>G
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NP_001253989.1:p.Ser224=
|
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