ENST00000261609.13:c.11814C>T
MANE Select
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ENSP00000261609.8:p.Asn3938=
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|
ENST00000650509.1:c.3525C>T
|
ENSP00000496936.1:p.Asn1175=
|
|
ENST00000261609.11:c.11814C>T
|
ENSP00000261609.7:p.Asn3938=
|
|
NM_004667.5:c.11814C>T
|
NP_004658.3:p.Asn3938=
|
|
XM_005268276.3:c.11700C>T
|
XP_005268333.1:p.Asn3900=
|
|
XM_005268277.3:c.11700C>T
|
XP_005268334.1:p.Asn3900=
|
|
XM_006720726.2:c.11799C>T
|
XP_006720789.1:p.Asn3933=
|
|
XM_006720727.2:c.11556C>T
|
XP_006720790.1:p.Asn3852=
|
|
XM_011522131.1:c.11331C>T
|
XP_011520433.1:p.Asn3777=
|
|
XM_011522132.1:c.9330C>T
|
XP_011520434.1:p.Asn3110=
|
|
XM_011522133.1:c.8559C>T
|
XP_011520435.1:p.Asn2853=
|
|
XM_011522134.1:c.5931C>T
|
XP_011520436.1:p.Asn1977=
|
|
XM_005268276.5:c.11700C>T
|
XP_005268333.1:p.Asn3900=
|
|
XM_006720726.3:c.11799C>T
|
XP_006720789.1:p.Asn3933=
|
|
XM_006720727.3:c.11556C>T
|
XP_006720790.1:p.Asn3852=
|
|
XM_017022695.1:c.11700C>T
|
XP_016878184.1:p.Asn3900=
|
|
XM_017022696.1:c.11700C>T
|
XP_016878185.1:p.Asn3900=
|
|
XM_017022697.1:c.4980C>T
|
XP_016878186.1:p.Asn1660=
|
|
XM_017022698.1:c.4980C>T
|
XP_016878187.1:p.Asn1660=
|
|
NM_004667.6:c.11814C>T
MANE Select
|
NP_004658.3:p.Asn3938=
|
|