ENST00000261609.13:c.11783A>G
MANE Select
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ENSP00000261609.8:p.Glu3928Gly
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ENST00000650509.1:c.3494A>G
|
ENSP00000496936.1:p.Glu1165Gly
|
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ENST00000261609.11:c.11783A>G
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ENSP00000261609.7:p.Glu3928Gly
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ENST00000564519.1:n.298A>G
|
|
|
NM_004667.5:c.11783A>G
|
NP_004658.3:p.Glu3928Gly
|
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XM_005268276.3:c.11669A>G
|
XP_005268333.1:p.Glu3890Gly
|
|
XM_005268277.3:c.11669A>G
|
XP_005268334.1:p.Glu3890Gly
|
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XM_006720726.2:c.11768A>G
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XP_006720789.1:p.Glu3923Gly
|
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XM_006720727.2:c.11525A>G
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XP_006720790.1:p.Glu3842Gly
|
|
XM_011522131.1:c.11300A>G
|
XP_011520433.1:p.Glu3767Gly
|
|
XM_011522132.1:c.9299A>G
|
XP_011520434.1:p.Glu3100Gly
|
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XM_011522133.1:c.8528A>G
|
XP_011520435.1:p.Glu2843Gly
|
|
XM_011522134.1:c.5900A>G
|
XP_011520436.1:p.Glu1967Gly
|
|
XM_005268276.5:c.11669A>G
|
XP_005268333.1:p.Glu3890Gly
|
|
XM_006720726.3:c.11768A>G
|
XP_006720789.1:p.Glu3923Gly
|
|
XM_006720727.3:c.11525A>G
|
XP_006720790.1:p.Glu3842Gly
|
|
XM_017022695.1:c.11669A>G
|
XP_016878184.1:p.Glu3890Gly
|
|
XM_017022696.1:c.11669A>G
|
XP_016878185.1:p.Glu3890Gly
|
|
XM_017022697.1:c.4949A>G
|
XP_016878186.1:p.Glu1650Gly
|
|
XM_017022698.1:c.4949A>G
|
XP_016878187.1:p.Glu1650Gly
|
|
NM_004667.6:c.11783A>G
MANE Select
|
NP_004658.3:p.Glu3928Gly
|
|