ENST00000310836.11:c.649A>C
MANE Select
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ENSP00000311648.6:p.Arg217=
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|
ENST00000310836.10:c.649A>C
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ENSP00000311648.6:p.Arg217=
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|
ENST00000394511.3:c.649A>C
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ENSP00000378019.3:p.Arg217=
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|
NM_001128174.1:c.649A>C
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NP_001121646.1:p.Arg217=
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|
NM_003360.3:c.649A>C
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NP_003351.2:p.Arg217=
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|
XM_006714302.2:c.649A>C
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XP_006714365.1:p.Arg217=
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|
XM_006714303.2:c.649A>C
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XP_006714366.1:p.Arg217=
|
|
XM_011532232.1:c.649A>C
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XP_011530534.1:p.Arg217=
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|
NM_001128174.2:c.649A>C
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NP_001121646.1:p.Arg217=
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|
NM_001322112.1:c.649A>C
|
NP_001309041.1:p.Arg217=
|
|
NM_001322113.1:c.649A>C
|
NP_001309042.1:p.Arg217=
|
|
NM_001322114.1:c.649A>C
|
NP_001309043.1:p.Arg217=
|
|
NM_003360.4:c.649A>C
|
NP_003351.2:p.Arg217=
|
|
XM_024454207.1:c.649A>C
|
XP_024309975.1:p.Arg217=
|
|
XM_024454208.1:c.649A>C
|
XP_024309976.1:p.Arg217=
|
|
XM_024454209.1:c.649A>C
|
XP_024309977.1:p.Arg217=
|
|
XM_024454210.1:c.649A>C
|
XP_024309978.1:p.Arg217=
|
|
XM_024454211.1:c.649A>C
|
XP_024309979.1:p.Arg217=
|
|
NM_001128174.3:c.649A>C
MANE Select
|
NP_001121646.2:p.Arg217=
|
|
NM_001322114.2:c.649A>C
|
NP_001309043.2:p.Arg217=
|
|
NM_003360.5:c.649A>C
|
NP_003351.3:p.Arg217=
|
|
NM_001322112.2:c.649A>C
|
NP_001309041.2:p.Arg217=
|
|
NM_001322113.2:c.649A>C
|
NP_001309042.2:p.Arg217=
|
|