ENST00000261609.13:c.11825A>C
MANE Select
|
ENSP00000261609.8:p.Asp3942Ala
|
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ENST00000650509.1:c.3536A>C
|
ENSP00000496936.1:p.Asp1179Ala
|
|
ENST00000261609.11:c.11825A>C
|
ENSP00000261609.7:p.Asp3942Ala
|
|
NM_004667.5:c.11825A>C
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NP_004658.3:p.Asp3942Ala
|
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XM_005268276.3:c.11711A>C
|
XP_005268333.1:p.Asp3904Ala
|
|
XM_005268277.3:c.11711A>C
|
XP_005268334.1:p.Asp3904Ala
|
|
XM_006720726.2:c.11810A>C
|
XP_006720789.1:p.Asp3937Ala
|
|
XM_006720727.2:c.11567A>C
|
XP_006720790.1:p.Asp3856Ala
|
|
XM_011522131.1:c.11342A>C
|
XP_011520433.1:p.Asp3781Ala
|
|
XM_011522132.1:c.9341A>C
|
XP_011520434.1:p.Asp3114Ala
|
|
XM_011522133.1:c.8570A>C
|
XP_011520435.1:p.Asp2857Ala
|
|
XM_011522134.1:c.5942A>C
|
XP_011520436.1:p.Asp1981Ala
|
|
XM_005268276.5:c.11711A>C
|
XP_005268333.1:p.Asp3904Ala
|
|
XM_006720726.3:c.11810A>C
|
XP_006720789.1:p.Asp3937Ala
|
|
XM_006720727.3:c.11567A>C
|
XP_006720790.1:p.Asp3856Ala
|
|
XM_017022695.1:c.11711A>C
|
XP_016878184.1:p.Asp3904Ala
|
|
XM_017022696.1:c.11711A>C
|
XP_016878185.1:p.Asp3904Ala
|
|
XM_017022697.1:c.4991A>C
|
XP_016878186.1:p.Asp1664Ala
|
|
XM_017022698.1:c.4991A>C
|
XP_016878187.1:p.Asp1664Ala
|
|
NM_004667.6:c.11825A>C
MANE Select
|
NP_004658.3:p.Asp3942Ala
|
|