ENST00000553106.6:c.659A>G
MANE Select
|
ENSP00000448059.1:p.His220Arg
|
|
ENST00000307000.7:c.644A>G
|
ENSP00000303500.2:p.His215Arg
|
|
ENST00000549111.5:n.755A>G
|
|
|
ENST00000553106.5:c.659A>G
|
ENSP00000448059.1:p.His220Arg
|
|
NM_000277.1:c.659A>G
|
NP_000268.1:p.His220Arg
|
|
XM_011538422.1:c.659A>G
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XP_011536724.1:p.His220Arg
|
|
NM_000277.2:c.659A>G
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NP_000268.1:p.His220Arg
|
|
NM_001354304.1:c.659A>G
|
NP_001341233.1:p.His220Arg
|
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XM_017019370.2:c.659A>G
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XP_016874859.1:p.His220Arg
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|
NM_000277.3:c.659A>G
MANE Select
|
NP_000268.1:p.His220Arg
|
|
NM_001354304.2:c.659A>G
|
NP_001341233.1:p.His220Arg
|
|