ENST00000261609.13:c.11815A>C
MANE Select
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ENSP00000261609.8:p.Arg3939=
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ENST00000650509.1:c.3526A>C
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ENSP00000496936.1:p.Arg1176=
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ENST00000261609.11:c.11815A>C
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ENSP00000261609.7:p.Arg3939=
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NM_004667.5:c.11815A>C
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NP_004658.3:p.Arg3939=
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XM_005268276.3:c.11701A>C
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XP_005268333.1:p.Arg3901=
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XM_005268277.3:c.11701A>C
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XP_005268334.1:p.Arg3901=
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XM_006720726.2:c.11800A>C
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XP_006720789.1:p.Arg3934=
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XM_006720727.2:c.11557A>C
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XP_006720790.1:p.Arg3853=
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XM_011522131.1:c.11332A>C
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XP_011520433.1:p.Arg3778=
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XM_011522132.1:c.9331A>C
|
XP_011520434.1:p.Arg3111=
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|
XM_011522133.1:c.8560A>C
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XP_011520435.1:p.Arg2854=
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XM_011522134.1:c.5932A>C
|
XP_011520436.1:p.Arg1978=
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|
XM_005268276.5:c.11701A>C
|
XP_005268333.1:p.Arg3901=
|
|
XM_006720726.3:c.11800A>C
|
XP_006720789.1:p.Arg3934=
|
|
XM_006720727.3:c.11557A>C
|
XP_006720790.1:p.Arg3853=
|
|
XM_017022695.1:c.11701A>C
|
XP_016878184.1:p.Arg3901=
|
|
XM_017022696.1:c.11701A>C
|
XP_016878185.1:p.Arg3901=
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XM_017022697.1:c.4981A>C
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XP_016878186.1:p.Arg1661=
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XM_017022698.1:c.4981A>C
|
XP_016878187.1:p.Arg1661=
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NM_004667.6:c.11815A>C
MANE Select
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NP_004658.3:p.Arg3939=
|
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