ENST00000262367.10:c.6926G>C
MANE Select
|
ENSP00000262367.5:p.Gly2309Ala
|
|
ENST00000262367.9:c.6926G>C
|
ENSP00000262367.5:p.Gly2309Ala
|
|
ENST00000382070.7:c.6812G>C
|
ENSP00000371502.3:p.Gly2271Ala
|
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NM_001079846.1:c.6812G>C
|
NP_001073315.1:p.Gly2271Ala
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NM_004380.2:c.6926G>C
|
NP_004371.2:p.Gly2309Ala
|
|
XM_005255124.3:c.6881G>C
|
XP_005255181.1:p.Gly2294Ala
|
|
XM_005255125.3:c.6509G>C
|
XP_005255182.1:p.Gly2170Ala
|
|
XM_006720848.2:c.6665G>C
|
XP_006720911.1:p.Gly2222Ala
|
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XM_011522380.1:c.6872G>C
|
XP_011520682.1:p.Gly2291Ala
|
|
XM_011522381.1:c.6173G>C
|
XP_011520683.1:p.Gly2058Ala
|
|
XM_005255124.4:c.6881G>C
|
XP_005255181.1:p.Gly2294Ala
|
|
XM_005255125.4:c.6509G>C
|
XP_005255182.1:p.Gly2170Ala
|
|
XM_006720848.3:c.6665G>C
|
XP_006720911.1:p.Gly2222Ala
|
|
XM_011522381.2:c.6173G>C
|
XP_011520683.1:p.Gly2058Ala
|
|
XM_017022944.1:c.6920G>C
|
XP_016878433.1:p.Gly2307Ala
|
|
NM_004380.3:c.6926G>C
MANE Select
|
NP_004371.2:p.Gly2309Ala
|
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