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NM_001369.3:c.7573G>A
MANE Select
|
NP_001360.1:p.Gly2525Arg
|
|
ENST00000265104.5:c.7573G>A
MANE Select
|
ENSP00000265104.4:p.Gly2525Arg
|
|
NM_001369.2:c.7573G>A
|
NP_001360.1:p.Gly2525Arg
|
|
ENST00000265104.4:c.7573G>A
|
ENSP00000265104.4:p.Gly2525Arg
|
|
ENST00000512443.1:n.429G>A
|
|
|
ENST00000681290.1:c.7528G>A
|
ENSP00000505288.1:p.Gly2510Arg
|
|
XM_005248262.2:c.7528G>A
|
XP_005248319.1:p.Gly2510Arg
|
|
XM_005248262.3:c.7681G>A
|
XP_005248319.2:p.Gly2561Arg
|
|
XM_011513990.1:c.7573G>A
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XP_011512292.1:p.Gly2525Arg
|
|
XM_017009177.1:c.7681G>A
|
XP_016864666.1:p.Gly2561Arg
|
|
XM_017009178.1:c.6586G>A
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XP_016864667.1:p.Gly2196Arg
|
|
XM_017009179.2:c.6586G>A
|
XP_016864668.1:p.Gly2196Arg
|
|
XM_017009180.1:c.7681G>A
|
XP_016864669.1:p.Gly2561Arg
|
|
XM_017009181.1:c.7681G>A
|
XP_016864670.1:p.Gly2561Arg
|
|
XM_017009182.1:c.7681G>A
|
XP_016864671.1:p.Gly2561Arg
|
|
XM_017009183.1:c.7681G>A
|
XP_016864672.1:p.Gly2561Arg
|
|
XM_017009184.1:c.7681G>A
|
XP_016864673.1:p.Gly2561Arg
|
|
XM_017009185.1:c.2770G>A
|
XP_016864674.1:p.Gly924Arg
|
|
XM_017009186.1:c.2323G>A
|
XP_016864675.1:p.Gly775Arg
|
|
XM_017009187.1:c.7681G>A
|
XP_016864676.1:p.Gly2561Arg
|
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XM_017009188.1:c.1660G>A
|
XP_016864677.1:p.Gly554Arg
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XM_024454388.1:c.6586G>A
|
XP_024310156.1:p.Gly2196Arg
|
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XM_024454389.1:c.6175G>A
|
XP_024310157.1:p.Gly2059Arg
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XR_001742034.1:n.7698G>A
|
|
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XR_001742035.1:n.7698G>A
|
|
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XR_925598.1:n.7780G>A
|
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