ENST00000261609.13:c.11801T>C
MANE Select
|
ENSP00000261609.8:p.Val3934Ala
|
|
ENST00000650509.1:c.3512T>C
|
ENSP00000496936.1:p.Val1171Ala
|
|
ENST00000261609.11:c.11801T>C
|
ENSP00000261609.7:p.Val3934Ala
|
|
ENST00000564519.1:n.316T>C
|
|
|
NM_004667.5:c.11801T>C
|
NP_004658.3:p.Val3934Ala
|
|
XM_005268276.3:c.11687T>C
|
XP_005268333.1:p.Val3896Ala
|
|
XM_005268277.3:c.11687T>C
|
XP_005268334.1:p.Val3896Ala
|
|
XM_006720726.2:c.11786T>C
|
XP_006720789.1:p.Val3929Ala
|
|
XM_006720727.2:c.11543T>C
|
XP_006720790.1:p.Val3848Ala
|
|
XM_011522131.1:c.11318T>C
|
XP_011520433.1:p.Val3773Ala
|
|
XM_011522132.1:c.9317T>C
|
XP_011520434.1:p.Val3106Ala
|
|
XM_011522133.1:c.8546T>C
|
XP_011520435.1:p.Val2849Ala
|
|
XM_011522134.1:c.5918T>C
|
XP_011520436.1:p.Val1973Ala
|
|
XM_005268276.5:c.11687T>C
|
XP_005268333.1:p.Val3896Ala
|
|
XM_006720726.3:c.11786T>C
|
XP_006720789.1:p.Val3929Ala
|
|
XM_006720727.3:c.11543T>C
|
XP_006720790.1:p.Val3848Ala
|
|
XM_017022695.1:c.11687T>C
|
XP_016878184.1:p.Val3896Ala
|
|
XM_017022696.1:c.11687T>C
|
XP_016878185.1:p.Val3896Ala
|
|
XM_017022697.1:c.4967T>C
|
XP_016878186.1:p.Val1656Ala
|
|
XM_017022698.1:c.4967T>C
|
XP_016878187.1:p.Val1656Ala
|
|
NM_004667.6:c.11801T>C
MANE Select
|
NP_004658.3:p.Val3934Ala
|
|