ENST00000298229.7:c.892C>G
MANE Select
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ENSP00000298229.2:p.Gln298Glu
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ENST00000298229.6:c.892C>G
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ENSP00000298229.2:p.Gln298Glu
|
|
ENST00000538751.5:c.166C>G
|
ENSP00000444619.1:p.Gln56Glu
|
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ENST00000540329.5:c.76C>G
|
ENSP00000440018.1:p.Gln26Glu
|
|
ENST00000541756.5:c.694C>G
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ENSP00000446360.2:p.Gln232Glu
|
|
NM_001567.3:c.892C>G
|
NP_001558.3:p.Gln298Glu
|
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XM_005273978.3:c.958C>G
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XP_005274035.1:p.Gln320Glu
|
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XM_005273979.3:c.958C>G
|
XP_005274036.1:p.Gln320Glu
|
|
XM_011544999.1:c.892C>G
|
XP_011543301.1:p.Gln298Glu
|
|
XM_011545000.1:c.958C>G
|
XP_011543302.1:p.Gln320Glu
|
|
XM_005273979.4:c.958C>G
|
XP_005274036.1:p.Gln320Glu
|
|
XM_011544999.2:c.892C>G
|
XP_011543301.1:p.Gln298Glu
|
|
XM_024448501.1:c.958C>G
|
XP_024304269.1:p.Gln320Glu
|
|
XM_024448502.1:c.958C>G
|
XP_024304270.1:p.Gln320Glu
|
|
XM_024448503.1:c.928C>G
|
XP_024304271.1:p.Gln310Glu
|
|
XM_024448504.1:c.892C>G
|
XP_024304272.1:p.Gln298Glu
|
|
XM_024448505.1:c.958C>G
|
XP_024304273.1:p.Gln320Glu
|
|
NM_001567.4:c.892C>G
MANE Select
|
NP_001558.3:p.Gln298Glu
|
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