ENST00000261609.13:c.11799T>G
MANE Select
|
ENSP00000261609.8:p.Leu3933=
|
|
ENST00000650509.1:c.3510T>G
|
ENSP00000496936.1:p.Leu1170=
|
|
ENST00000261609.11:c.11799T>G
|
ENSP00000261609.7:p.Leu3933=
|
|
ENST00000564519.1:n.314T>G
|
|
|
NM_004667.5:c.11799T>G
|
NP_004658.3:p.Leu3933=
|
|
XM_005268276.3:c.11685T>G
|
XP_005268333.1:p.Leu3895=
|
|
XM_005268277.3:c.11685T>G
|
XP_005268334.1:p.Leu3895=
|
|
XM_006720726.2:c.11784T>G
|
XP_006720789.1:p.Leu3928=
|
|
XM_006720727.2:c.11541T>G
|
XP_006720790.1:p.Leu3847=
|
|
XM_011522131.1:c.11316T>G
|
XP_011520433.1:p.Leu3772=
|
|
XM_011522132.1:c.9315T>G
|
XP_011520434.1:p.Leu3105=
|
|
XM_011522133.1:c.8544T>G
|
XP_011520435.1:p.Leu2848=
|
|
XM_011522134.1:c.5916T>G
|
XP_011520436.1:p.Leu1972=
|
|
XM_005268276.5:c.11685T>G
|
XP_005268333.1:p.Leu3895=
|
|
XM_006720726.3:c.11784T>G
|
XP_006720789.1:p.Leu3928=
|
|
XM_006720727.3:c.11541T>G
|
XP_006720790.1:p.Leu3847=
|
|
XM_017022695.1:c.11685T>G
|
XP_016878184.1:p.Leu3895=
|
|
XM_017022696.1:c.11685T>G
|
XP_016878185.1:p.Leu3895=
|
|
XM_017022697.1:c.4965T>G
|
XP_016878186.1:p.Leu1655=
|
|
XM_017022698.1:c.4965T>G
|
XP_016878187.1:p.Leu1655=
|
|
NM_004667.6:c.11799T>G
MANE Select
|
NP_004658.3:p.Leu3933=
|
|