ENST00000261609.13:c.11851A>G
MANE Select
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ENSP00000261609.8:p.Ser3951Gly
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ENST00000650509.1:c.3562A>G
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ENSP00000496936.1:p.Ser1188Gly
|
|
ENST00000261609.11:c.11851A>G
|
ENSP00000261609.7:p.Ser3951Gly
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|
NM_004667.5:c.11851A>G
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NP_004658.3:p.Ser3951Gly
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XM_005268276.3:c.11737A>G
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XP_005268333.1:p.Ser3913Gly
|
|
XM_005268277.3:c.11737A>G
|
XP_005268334.1:p.Ser3913Gly
|
|
XM_006720726.2:c.11836A>G
|
XP_006720789.1:p.Ser3946Gly
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XM_006720727.2:c.11593A>G
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XP_006720790.1:p.Ser3865Gly
|
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XM_011522131.1:c.11368A>G
|
XP_011520433.1:p.Ser3790Gly
|
|
XM_011522132.1:c.9367A>G
|
XP_011520434.1:p.Ser3123Gly
|
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XM_011522133.1:c.8596A>G
|
XP_011520435.1:p.Ser2866Gly
|
|
XM_011522134.1:c.5968A>G
|
XP_011520436.1:p.Ser1990Gly
|
|
XM_005268276.5:c.11737A>G
|
XP_005268333.1:p.Ser3913Gly
|
|
XM_006720726.3:c.11836A>G
|
XP_006720789.1:p.Ser3946Gly
|
|
XM_006720727.3:c.11593A>G
|
XP_006720790.1:p.Ser3865Gly
|
|
XM_017022695.1:c.11737A>G
|
XP_016878184.1:p.Ser3913Gly
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|
XM_017022696.1:c.11737A>G
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XP_016878185.1:p.Ser3913Gly
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|
XM_017022697.1:c.5017A>G
|
XP_016878186.1:p.Ser1673Gly
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|
XM_017022698.1:c.5017A>G
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XP_016878187.1:p.Ser1673Gly
|
|
NM_004667.6:c.11851A>G
MANE Select
|
NP_004658.3:p.Ser3951Gly
|
|