ENST00000233575.7:c.682A>T
MANE Select
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ENSP00000233575.2:p.Thr228Ser
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ENST00000233575.6:c.682A>T
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ENSP00000233575.2:p.Thr228Ser
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ENST00000427123.5:c.*492A>T
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ENSP00000405399.1:n.*492A>T
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ENST00000440760.5:c.*527A>T
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ENSP00000399727.1:n.*527A>T
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ENST00000453453.1:c.*209A>T
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ENSP00000401922.1:n.*209A>T
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ENST00000493711.1:n.399A>T
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|
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ENST00000494893.5:n.858A>T
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|
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ENST00000537606.5:c.607A>T
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ENSP00000439208.1:p.Thr203Ser
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NM_001267059.1:c.646A>T
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NP_001253988.1:p.Thr216Ser
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NM_001267060.1:c.607A>T
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NP_001253989.1:p.Thr203Ser
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|
NM_001267061.1:c.622A>T
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NP_001253990.1:p.Thr208Ser
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NM_014748.3:c.682A>T
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NP_055563.1:p.Thr228Ser
|
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NR_049782.1:n.1055A>T
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|
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NR_049783.1:n.1028A>T
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|
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NR_049784.1:n.1004A>T
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|
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NR_049785.1:n.937A>T
|
|
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NR_049786.1:n.886A>T
|
|
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NR_049787.1:n.737A>T
|
|
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NR_049788.1:n.667A>T
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|
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XM_011533203.1:c.40A>T
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XP_011531505.1:p.Thr14Ser
|
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XM_011533203.2:c.40A>T
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XP_011531505.1:p.Thr14Ser
|
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XM_017005405.2:c.40A>T
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XP_016860894.1:p.Thr14Ser
|
|
NM_014748.4:c.682A>T
MANE Select
|
NP_055563.1:p.Thr228Ser
|
|
NM_001267059.2:c.646A>T
|
NP_001253988.1:p.Thr216Ser
|
|
NM_001267061.2:c.622A>T
|
NP_001253990.1:p.Thr208Ser
|
|
NR_049782.2:n.935A>T
|
|
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NR_049783.2:n.908A>T
|
|
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NR_049784.2:n.884A>T
|
|
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NR_049785.2:n.817A>T
|
|
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NR_049786.2:n.766A>T
|
|
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NR_049787.2:n.617A>T
|
|
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NR_049788.2:n.547A>T
|
|
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NM_001267060.2:c.607A>T
|
NP_001253989.1:p.Thr203Ser
|
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