ENST00000394975.3:c.480T>G
MANE Select
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ENSP00000378426.2:p.Ala160=
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ENST00000300851.10:c.*91T>G
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ENSP00000300851.6:n.*91T>G
|
|
ENST00000319788.11:c.*91T>G
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ENSP00000326135.7:n.*91T>G
|
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ENST00000354895.4:c.*91T>G
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ENSP00000346969.4:n.*91T>G
|
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ENST00000394971.7:c.*91T>G
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ENSP00000378422.3:n.*91T>G
|
|
ENST00000394975.2:c.480T>G
|
ENSP00000378426.2:p.Ala160=
|
|
ENST00000420057.2:c.442T>G
|
|
|
ENST00000529564.1:c.283+2166T>G
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ENSP00000431371.1:n.283+2166T>G
|
|
ENST00000532364.1:c.173+3411T>G
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ENSP00000460316.1:n.173+3411T>G
|
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ENST00000533518.5:c.353T>G
|
|
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NM_001311311.1:c.564T>G
|
NP_001298240.1:p.Ala188=
|
|
NM_024006.4:c.480T>G
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NP_076869.1:p.Ala160=
|
|
NM_024006.5:c.480T>G
|
NP_076869.1:p.Ala160=
|
|
NM_206824.1:c.*91T>G
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NP_996560.1:n.*91T>G
|
|
NM_206824.2:c.*91T>G
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NP_996560.1:n.*91T>G
|
|
XM_011545944.1:c.480T>G
|
XP_011544246.1:p.Ala160=
|
|
XM_011545945.1:c.*91T>G
|
XP_011544247.1:n.*91T>G
|
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XR_950848.1:n.1268T>G
|
|
|
NM_024006.6:c.480T>G
MANE Select
|
NP_076869.1:p.Ala160=
|
|
NM_001311311.2:c.564T>G
|
NP_001298240.1:p.Ala188=
|
|
NM_206824.3:c.*91T>G
|
NP_996560.1:n.*91T>G
|
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