ENST00000281928.9:c.2781G=
MANE Select
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ENSP00000281928.3:p.Glu927=
|
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ENST00000548743.2:c.2751G=
|
ENSP00000448553.2:p.Glu917=
|
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ENST00000549786.2:c.2209G=
|
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ENST00000647927.1:n.3154G=
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|
ENST00000648173.1:n.1576G=
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ENST00000648379.1:n.1149G=
|
|
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ENST00000648737.1:n.2545G=
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ENST00000648916.1:n.792G=
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|
|
ENST00000649607.1:c.965G=
|
|
|
ENST00000650226.1:c.2781G=
|
ENSP00000496981.1:p.Glu927=
|
|
ENST00000281928.7:c.2781G=
|
ENSP00000281928.3:p.Glu927=
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|
NM_015335.4:c.2781G=
|
NP_056150.1:p.Glu927=
|
|
XM_011538080.1:c.2781G=
|
XP_011536382.1:p.Glu927=
|
|
XM_011538081.1:c.2778G=
|
XP_011536383.1:p.Glu926=
|
|
XM_011538082.1:c.2751G=
|
XP_011536384.1:p.Glu917=
|
|
XM_011538080.2:c.2781G=
|
XP_011536382.1:p.Glu927=
|
|
XM_011538081.2:c.2778G=
|
XP_011536383.1:p.Glu926=
|
|
XM_011538082.2:c.2751G=
|
XP_011536384.1:p.Glu917=
|
|
XM_017019090.1:c.2778G=
|
XP_016874579.1:p.Glu926=
|
|
NM_015335.5:c.2781G=
MANE Select
|
NP_056150.1:p.Glu927=
|
|