ENST00000261609.13:c.11749G>T
MANE Select
|
ENSP00000261609.8:p.Val3917Phe
|
|
ENST00000650509.1:c.3460G>T
|
ENSP00000496936.1:p.Val1154Phe
|
|
ENST00000261609.11:c.11749G>T
|
ENSP00000261609.7:p.Val3917Phe
|
|
ENST00000564519.1:n.264G>T
|
|
|
NM_004667.5:c.11749G>T
|
NP_004658.3:p.Val3917Phe
|
|
XM_005268276.3:c.11635G>T
|
XP_005268333.1:p.Val3879Phe
|
|
XM_005268277.3:c.11635G>T
|
XP_005268334.1:p.Val3879Phe
|
|
XM_006720726.2:c.11734G>T
|
XP_006720789.1:p.Val3912Phe
|
|
XM_006720727.2:c.11491G>T
|
XP_006720790.1:p.Val3831Phe
|
|
XM_011522131.1:c.11266G>T
|
XP_011520433.1:p.Val3756Phe
|
|
XM_011522132.1:c.9265G>T
|
XP_011520434.1:p.Val3089Phe
|
|
XM_011522133.1:c.8494G>T
|
XP_011520435.1:p.Val2832Phe
|
|
XM_011522134.1:c.5866G>T
|
XP_011520436.1:p.Val1956Phe
|
|
XM_005268276.5:c.11635G>T
|
XP_005268333.1:p.Val3879Phe
|
|
XM_006720726.3:c.11734G>T
|
XP_006720789.1:p.Val3912Phe
|
|
XM_006720727.3:c.11491G>T
|
XP_006720790.1:p.Val3831Phe
|
|
XM_017022695.1:c.11635G>T
|
XP_016878184.1:p.Val3879Phe
|
|
XM_017022696.1:c.11635G>T
|
XP_016878185.1:p.Val3879Phe
|
|
XM_017022697.1:c.4915G>T
|
XP_016878186.1:p.Val1639Phe
|
|
XM_017022698.1:c.4915G>T
|
XP_016878187.1:p.Val1639Phe
|
|
NM_004667.6:c.11749G>T
MANE Select
|
NP_004658.3:p.Val3917Phe
|
|