ENST00000261609.13:c.11722T>C
MANE Select
|
ENSP00000261609.8:p.Leu3908=
|
|
ENST00000650509.1:c.3433T>C
|
ENSP00000496936.1:p.Leu1145=
|
|
ENST00000261609.11:c.11722T>C
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ENSP00000261609.7:p.Leu3908=
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|
ENST00000564519.1:n.237T>C
|
|
|
NM_004667.5:c.11722T>C
|
NP_004658.3:p.Leu3908=
|
|
XM_005268276.3:c.11608T>C
|
XP_005268333.1:p.Leu3870=
|
|
XM_005268277.3:c.11608T>C
|
XP_005268334.1:p.Leu3870=
|
|
XM_006720726.2:c.11707T>C
|
XP_006720789.1:p.Leu3903=
|
|
XM_006720727.2:c.11464T>C
|
XP_006720790.1:p.Leu3822=
|
|
XM_011522131.1:c.11239T>C
|
XP_011520433.1:p.Leu3747=
|
|
XM_011522132.1:c.9238T>C
|
XP_011520434.1:p.Leu3080=
|
|
XM_011522133.1:c.8467T>C
|
XP_011520435.1:p.Leu2823=
|
|
XM_011522134.1:c.5839T>C
|
XP_011520436.1:p.Leu1947=
|
|
XM_005268276.5:c.11608T>C
|
XP_005268333.1:p.Leu3870=
|
|
XM_006720726.3:c.11707T>C
|
XP_006720789.1:p.Leu3903=
|
|
XM_006720727.3:c.11464T>C
|
XP_006720790.1:p.Leu3822=
|
|
XM_017022695.1:c.11608T>C
|
XP_016878184.1:p.Leu3870=
|
|
XM_017022696.1:c.11608T>C
|
XP_016878185.1:p.Leu3870=
|
|
XM_017022697.1:c.4888T>C
|
XP_016878186.1:p.Leu1630=
|
|
XM_017022698.1:c.4888T>C
|
XP_016878187.1:p.Leu1630=
|
|
NM_004667.6:c.11722T>C
MANE Select
|
NP_004658.3:p.Leu3908=
|
|