ENST00000233575.7:c.803A>T
MANE Select
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ENSP00000233575.2:p.His268Leu
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ENST00000233575.6:c.803A>T
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ENSP00000233575.2:p.His268Leu
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ENST00000427123.5:c.*613A>T
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ENSP00000405399.1:n.*613A>T
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ENST00000440760.5:c.*648A>T
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ENSP00000399727.1:n.*648A>T
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ENST00000453453.1:c.*330A>T
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ENSP00000401922.1:n.*330A>T
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ENST00000493711.1:n.520A>T
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ENST00000537606.5:c.728A>T
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ENSP00000439208.1:p.His243Leu
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NM_001267059.1:c.767A>T
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NP_001253988.1:p.His256Leu
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NM_001267060.1:c.728A>T
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NP_001253989.1:p.His243Leu
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NM_001267061.1:c.743A>T
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NP_001253990.1:p.His248Leu
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NM_014748.3:c.803A>T
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NP_055563.1:p.His268Leu
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NR_049782.1:n.1176A>T
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|
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NR_049783.1:n.1149A>T
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|
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NR_049784.1:n.1125A>T
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NR_049785.1:n.1058A>T
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NR_049786.1:n.1007A>T
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NR_049787.1:n.858A>T
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|
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NR_049788.1:n.788A>T
|
|
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XM_011533203.1:c.161A>T
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XP_011531505.1:p.His54Leu
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XM_011533203.2:c.161A>T
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XP_011531505.1:p.His54Leu
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XM_017005405.2:c.161A>T
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XP_016860894.1:p.His54Leu
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NM_014748.4:c.803A>T
MANE Select
|
NP_055563.1:p.His268Leu
|
|
NM_001267059.2:c.767A>T
|
NP_001253988.1:p.His256Leu
|
|
NM_001267061.2:c.743A>T
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NP_001253990.1:p.His248Leu
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NR_049782.2:n.1056A>T
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|
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NR_049783.2:n.1029A>T
|
|
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NR_049784.2:n.1005A>T
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NR_049785.2:n.938A>T
|
|
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NR_049786.2:n.887A>T
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|
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NR_049787.2:n.738A>T
|
|
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NR_049788.2:n.668A>T
|
|
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NM_001267060.2:c.728A>T
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NP_001253989.1:p.His243Leu
|
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