ENST00000375731.9:c.830A>C
MANE Select
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ENSP00000364883.5:p.Glu277Ala
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ENST00000303617.5:c.743A>C
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ENSP00000307334.5:p.Glu248Ala
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ENST00000375731.8:c.830A>C
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ENSP00000364883.4:p.Glu277Ala
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ENST00000473695.1:n.102A>C
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NM_001306190.1:c.743A>C
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NP_001293119.1:p.Glu248Ala
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NM_001698.2:c.830A>C , LRG_449t1:c.830A>C
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NP_001689.1:p.Glu277Ala
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XM_005252066.2:c.860A>C
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XP_005252123.1:p.Glu287Ala
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XM_005252067.3:c.860A>C
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XP_005252124.1:p.Glu287Ala
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XM_005252069.3:c.860A>C
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XP_005252126.1:p.Glu287Ala
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XM_005252073.2:c.368A>C
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XP_005252130.1:p.Glu123Ala
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XM_006717150.2:c.773A>C
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XP_006717213.1:p.Glu258Ala
|
|
XM_011518801.1:c.506A>C
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XP_011517103.1:p.Glu169Ala
|
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XM_011518802.1:c.503A>C
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XP_011517104.1:p.Glu168Ala
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NM_001351431.1:c.503A>C
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NP_001338360.1:p.Glu168Ala
|
|
NM_001351432.1:c.503A>C
|
NP_001338361.1:p.Glu168Ala
|
|
NM_001351433.1:c.503A>C
|
NP_001338362.1:p.Glu168Ala
|
|
XM_005252066.3:c.860A>C
|
XP_005252123.1:p.Glu287Ala
|
|
XM_005252067.4:c.860A>C
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XP_005252124.1:p.Glu287Ala
|
|
XM_005252069.4:c.860A>C
|
XP_005252126.1:p.Glu287Ala
|
|
XM_006717150.3:c.773A>C
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XP_006717213.1:p.Glu258Ala
|
|
XM_017014849.1:c.830A>C
|
XP_016870338.1:p.Glu277Ala
|
|
XR_001746328.2:n.1055A>C
|
|
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XR_001746329.2:n.1007A>C
|
|
|
NM_001698.3:c.830A>C
MANE Select
|
NP_001689.1:p.Glu277Ala
|
|
NM_001306190.2:c.743A>C
|
NP_001293119.1:p.Glu248Ala
|
|
NM_001351431.2:c.503A>C
|
NP_001338360.1:p.Glu168Ala
|
|
NM_001351432.2:c.503A>C
|
NP_001338361.1:p.Glu168Ala
|
|
NM_001351433.2:c.503A>C
|
NP_001338362.1:p.Glu168Ala
|
|