ENST00000295754.10:c.710A>G
MANE Select
|
ENSP00000295754.5:p.His237Arg
|
|
ENST00000672866.1:n.2306A>G
|
|
|
ENST00000295754.9:c.710A>G
|
ENSP00000295754.5:p.His237Arg
|
|
ENST00000359013.4:c.785A>G
|
ENSP00000351905.4:p.His262Arg
|
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NM_001024847.2:c.785A>G , LRG_779t1:c.785A>G
|
NP_001020018.1:p.His262Arg
|
|
NM_003242.5:c.710A>G
|
NP_003233.4:p.His237Arg
|
|
XM_011534043.1:c.737A>G
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XP_011532345.1:p.His246Arg
|
|
XM_011534044.1:c.662A>G
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XP_011532346.1:p.His221Arg
|
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XM_011534045.1:c.605A>G
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XP_011532347.1:p.His202Arg
|
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XM_011534043.2:c.737A>G
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XP_011532345.1:p.His246Arg
|
|
XM_011534045.3:c.605A>G
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XP_011532347.1:p.His202Arg
|
|
XM_017007106.1:c.605A>G
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XP_016862595.1:p.His202Arg
|
|
NM_003242.6:c.710A>G
MANE Select
|
NP_003233.4:p.His237Arg
|
|