ENST00000261609.13:c.11918T>C
MANE Select
|
ENSP00000261609.8:p.Val3973Ala
|
|
ENST00000650509.1:c.3629T>C
|
ENSP00000496936.1:p.Val1210Ala
|
|
ENST00000261609.11:c.11918T>C
|
ENSP00000261609.7:p.Val3973Ala
|
|
NM_004667.5:c.11918T>C
|
NP_004658.3:p.Val3973Ala
|
|
XM_005268276.3:c.11804T>C
|
XP_005268333.1:p.Val3935Ala
|
|
XM_005268277.3:c.11804T>C
|
XP_005268334.1:p.Val3935Ala
|
|
XM_006720726.2:c.11903T>C
|
XP_006720789.1:p.Val3968Ala
|
|
XM_006720727.2:c.11660T>C
|
XP_006720790.1:p.Val3887Ala
|
|
XM_011522131.1:c.11435T>C
|
XP_011520433.1:p.Val3812Ala
|
|
XM_011522132.1:c.9434T>C
|
XP_011520434.1:p.Val3145Ala
|
|
XM_011522133.1:c.8663T>C
|
XP_011520435.1:p.Val2888Ala
|
|
XM_011522134.1:c.6035T>C
|
XP_011520436.1:p.Val2012Ala
|
|
XM_005268276.5:c.11804T>C
|
XP_005268333.1:p.Val3935Ala
|
|
XM_006720726.3:c.11903T>C
|
XP_006720789.1:p.Val3968Ala
|
|
XM_006720727.3:c.11660T>C
|
XP_006720790.1:p.Val3887Ala
|
|
XM_017022695.1:c.11804T>C
|
XP_016878184.1:p.Val3935Ala
|
|
XM_017022696.1:c.11804T>C
|
XP_016878185.1:p.Val3935Ala
|
|
XM_017022697.1:c.5084T>C
|
XP_016878186.1:p.Val1695Ala
|
|
XM_017022698.1:c.5084T>C
|
XP_016878187.1:p.Val1695Ala
|
|
NM_004667.6:c.11918T>C
MANE Select
|
NP_004658.3:p.Val3973Ala
|
|