ENST00000261609.13:c.11711A>C
MANE Select
|
ENSP00000261609.8:p.Lys3904Thr
|
|
ENST00000650509.1:c.3422A>C
|
ENSP00000496936.1:p.Lys1141Thr
|
|
ENST00000261609.11:c.11711A>C
|
ENSP00000261609.7:p.Lys3904Thr
|
|
ENST00000564519.1:n.226A>C
|
|
|
NM_004667.5:c.11711A>C
|
NP_004658.3:p.Lys3904Thr
|
|
XM_005268276.3:c.11597A>C
|
XP_005268333.1:p.Lys3866Thr
|
|
XM_005268277.3:c.11597A>C
|
XP_005268334.1:p.Lys3866Thr
|
|
XM_006720726.2:c.11696A>C
|
XP_006720789.1:p.Lys3899Thr
|
|
XM_006720727.2:c.11453A>C
|
XP_006720790.1:p.Lys3818Thr
|
|
XM_011522131.1:c.11228A>C
|
XP_011520433.1:p.Lys3743Thr
|
|
XM_011522132.1:c.9227A>C
|
XP_011520434.1:p.Lys3076Thr
|
|
XM_011522133.1:c.8456A>C
|
XP_011520435.1:p.Lys2819Thr
|
|
XM_011522134.1:c.5828A>C
|
XP_011520436.1:p.Lys1943Thr
|
|
XM_005268276.5:c.11597A>C
|
XP_005268333.1:p.Lys3866Thr
|
|
XM_006720726.3:c.11696A>C
|
XP_006720789.1:p.Lys3899Thr
|
|
XM_006720727.3:c.11453A>C
|
XP_006720790.1:p.Lys3818Thr
|
|
XM_017022695.1:c.11597A>C
|
XP_016878184.1:p.Lys3866Thr
|
|
XM_017022696.1:c.11597A>C
|
XP_016878185.1:p.Lys3866Thr
|
|
XM_017022697.1:c.4877A>C
|
XP_016878186.1:p.Lys1626Thr
|
|
XM_017022698.1:c.4877A>C
|
XP_016878187.1:p.Lys1626Thr
|
|
NM_004667.6:c.11711A>C
MANE Select
|
NP_004658.3:p.Lys3904Thr
|
|