ENST00000233575.7:c.807T>G
MANE Select
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ENSP00000233575.2:p.Tyr269Ter
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ENST00000233575.6:c.807T>G
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ENSP00000233575.2:p.Tyr269Ter
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ENST00000427123.5:c.*617T>G
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ENSP00000405399.1:n.*617T>G
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ENST00000440760.5:c.*652T>G
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ENSP00000399727.1:n.*652T>G
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ENST00000453453.1:c.*334T>G
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ENSP00000401922.1:n.*334T>G
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ENST00000493711.1:n.524T>G
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|
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ENST00000537606.5:c.732T>G
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ENSP00000439208.1:p.Tyr244Ter
|
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NM_001267059.1:c.771T>G
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NP_001253988.1:p.Tyr257Ter
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NM_001267060.1:c.732T>G
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NP_001253989.1:p.Tyr244Ter
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NM_001267061.1:c.747T>G
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NP_001253990.1:p.Tyr249Ter
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NM_014748.3:c.807T>G
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NP_055563.1:p.Tyr269Ter
|
|
NR_049782.1:n.1180T>G
|
|
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NR_049783.1:n.1153T>G
|
|
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NR_049784.1:n.1129T>G
|
|
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NR_049785.1:n.1062T>G
|
|
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NR_049786.1:n.1011T>G
|
|
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NR_049787.1:n.862T>G
|
|
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NR_049788.1:n.792T>G
|
|
|
XM_011533203.1:c.165T>G
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XP_011531505.1:p.Tyr55Ter
|
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XM_011533203.2:c.165T>G
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XP_011531505.1:p.Tyr55Ter
|
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XM_017005405.2:c.165T>G
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XP_016860894.1:p.Tyr55Ter
|
|
NM_014748.4:c.807T>G
MANE Select
|
NP_055563.1:p.Tyr269Ter
|
|
NM_001267059.2:c.771T>G
|
NP_001253988.1:p.Tyr257Ter
|
|
NM_001267061.2:c.747T>G
|
NP_001253990.1:p.Tyr249Ter
|
|
NR_049782.2:n.1060T>G
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|
|
NR_049783.2:n.1033T>G
|
|
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NR_049784.2:n.1009T>G
|
|
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NR_049785.2:n.942T>G
|
|
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NR_049786.2:n.891T>G
|
|
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NR_049787.2:n.742T>G
|
|
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NR_049788.2:n.672T>G
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|
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NM_001267060.2:c.732T>G
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NP_001253989.1:p.Tyr244Ter
|
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