ENST00000261609.13:c.11714T>C
MANE Select
|
ENSP00000261609.8:p.Ile3905Thr
|
|
ENST00000650509.1:c.3425T>C
|
ENSP00000496936.1:p.Ile1142Thr
|
|
ENST00000261609.11:c.11714T>C
|
ENSP00000261609.7:p.Ile3905Thr
|
|
ENST00000564519.1:n.229T>C
|
|
|
NM_004667.5:c.11714T>C
|
NP_004658.3:p.Ile3905Thr
|
|
XM_005268276.3:c.11600T>C
|
XP_005268333.1:p.Ile3867Thr
|
|
XM_005268277.3:c.11600T>C
|
XP_005268334.1:p.Ile3867Thr
|
|
XM_006720726.2:c.11699T>C
|
XP_006720789.1:p.Ile3900Thr
|
|
XM_006720727.2:c.11456T>C
|
XP_006720790.1:p.Ile3819Thr
|
|
XM_011522131.1:c.11231T>C
|
XP_011520433.1:p.Ile3744Thr
|
|
XM_011522132.1:c.9230T>C
|
XP_011520434.1:p.Ile3077Thr
|
|
XM_011522133.1:c.8459T>C
|
XP_011520435.1:p.Ile2820Thr
|
|
XM_011522134.1:c.5831T>C
|
XP_011520436.1:p.Ile1944Thr
|
|
XM_005268276.5:c.11600T>C
|
XP_005268333.1:p.Ile3867Thr
|
|
XM_006720726.3:c.11699T>C
|
XP_006720789.1:p.Ile3900Thr
|
|
XM_006720727.3:c.11456T>C
|
XP_006720790.1:p.Ile3819Thr
|
|
XM_017022695.1:c.11600T>C
|
XP_016878184.1:p.Ile3867Thr
|
|
XM_017022696.1:c.11600T>C
|
XP_016878185.1:p.Ile3867Thr
|
|
XM_017022697.1:c.4880T>C
|
XP_016878186.1:p.Ile1627Thr
|
|
XM_017022698.1:c.4880T>C
|
XP_016878187.1:p.Ile1627Thr
|
|
NM_004667.6:c.11714T>C
MANE Select
|
NP_004658.3:p.Ile3905Thr
|
|