ENST00000261609.13:c.11761A>G
MANE Select
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ENSP00000261609.8:p.Ser3921Gly
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ENST00000650509.1:c.3472A>G
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ENSP00000496936.1:p.Ser1158Gly
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ENST00000261609.11:c.11761A>G
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ENSP00000261609.7:p.Ser3921Gly
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ENST00000564519.1:n.276A>G
|
|
|
NM_004667.5:c.11761A>G
|
NP_004658.3:p.Ser3921Gly
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XM_005268276.3:c.11647A>G
|
XP_005268333.1:p.Ser3883Gly
|
|
XM_005268277.3:c.11647A>G
|
XP_005268334.1:p.Ser3883Gly
|
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XM_006720726.2:c.11746A>G
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XP_006720789.1:p.Ser3916Gly
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XM_006720727.2:c.11503A>G
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XP_006720790.1:p.Ser3835Gly
|
|
XM_011522131.1:c.11278A>G
|
XP_011520433.1:p.Ser3760Gly
|
|
XM_011522132.1:c.9277A>G
|
XP_011520434.1:p.Ser3093Gly
|
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XM_011522133.1:c.8506A>G
|
XP_011520435.1:p.Ser2836Gly
|
|
XM_011522134.1:c.5878A>G
|
XP_011520436.1:p.Ser1960Gly
|
|
XM_005268276.5:c.11647A>G
|
XP_005268333.1:p.Ser3883Gly
|
|
XM_006720726.3:c.11746A>G
|
XP_006720789.1:p.Ser3916Gly
|
|
XM_006720727.3:c.11503A>G
|
XP_006720790.1:p.Ser3835Gly
|
|
XM_017022695.1:c.11647A>G
|
XP_016878184.1:p.Ser3883Gly
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|
XM_017022696.1:c.11647A>G
|
XP_016878185.1:p.Ser3883Gly
|
|
XM_017022697.1:c.4927A>G
|
XP_016878186.1:p.Ser1643Gly
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|
XM_017022698.1:c.4927A>G
|
XP_016878187.1:p.Ser1643Gly
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|
NM_004667.6:c.11761A>G
MANE Select
|
NP_004658.3:p.Ser3921Gly
|
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