ENST00000261609.13:c.11708A>C
MANE Select
|
ENSP00000261609.8:p.Lys3903Thr
|
|
ENST00000650509.1:c.3419A>C
|
ENSP00000496936.1:p.Lys1140Thr
|
|
ENST00000261609.11:c.11708A>C
|
ENSP00000261609.7:p.Lys3903Thr
|
|
ENST00000564519.1:n.223A>C
|
|
|
NM_004667.5:c.11708A>C
|
NP_004658.3:p.Lys3903Thr
|
|
XM_005268276.3:c.11594A>C
|
XP_005268333.1:p.Lys3865Thr
|
|
XM_005268277.3:c.11594A>C
|
XP_005268334.1:p.Lys3865Thr
|
|
XM_006720726.2:c.11693A>C
|
XP_006720789.1:p.Lys3898Thr
|
|
XM_006720727.2:c.11450A>C
|
XP_006720790.1:p.Lys3817Thr
|
|
XM_011522131.1:c.11225A>C
|
XP_011520433.1:p.Lys3742Thr
|
|
XM_011522132.1:c.9224A>C
|
XP_011520434.1:p.Lys3075Thr
|
|
XM_011522133.1:c.8453A>C
|
XP_011520435.1:p.Lys2818Thr
|
|
XM_011522134.1:c.5825A>C
|
XP_011520436.1:p.Lys1942Thr
|
|
XM_005268276.5:c.11594A>C
|
XP_005268333.1:p.Lys3865Thr
|
|
XM_006720726.3:c.11693A>C
|
XP_006720789.1:p.Lys3898Thr
|
|
XM_006720727.3:c.11450A>C
|
XP_006720790.1:p.Lys3817Thr
|
|
XM_017022695.1:c.11594A>C
|
XP_016878184.1:p.Lys3865Thr
|
|
XM_017022696.1:c.11594A>C
|
XP_016878185.1:p.Lys3865Thr
|
|
XM_017022697.1:c.4874A>C
|
XP_016878186.1:p.Lys1625Thr
|
|
XM_017022698.1:c.4874A>C
|
XP_016878187.1:p.Lys1625Thr
|
|
NM_004667.6:c.11708A>C
MANE Select
|
NP_004658.3:p.Lys3903Thr
|
|