ENST00000261609.13:c.11728G>T
MANE Select
|
ENSP00000261609.8:p.Ala3910Ser
|
|
ENST00000650509.1:c.3439G>T
|
ENSP00000496936.1:p.Ala1147Ser
|
|
ENST00000261609.11:c.11728G>T
|
ENSP00000261609.7:p.Ala3910Ser
|
|
ENST00000564519.1:n.243G>T
|
|
|
NM_004667.5:c.11728G>T
|
NP_004658.3:p.Ala3910Ser
|
|
XM_005268276.3:c.11614G>T
|
XP_005268333.1:p.Ala3872Ser
|
|
XM_005268277.3:c.11614G>T
|
XP_005268334.1:p.Ala3872Ser
|
|
XM_006720726.2:c.11713G>T
|
XP_006720789.1:p.Ala3905Ser
|
|
XM_006720727.2:c.11470G>T
|
XP_006720790.1:p.Ala3824Ser
|
|
XM_011522131.1:c.11245G>T
|
XP_011520433.1:p.Ala3749Ser
|
|
XM_011522132.1:c.9244G>T
|
XP_011520434.1:p.Ala3082Ser
|
|
XM_011522133.1:c.8473G>T
|
XP_011520435.1:p.Ala2825Ser
|
|
XM_011522134.1:c.5845G>T
|
XP_011520436.1:p.Ala1949Ser
|
|
XM_005268276.5:c.11614G>T
|
XP_005268333.1:p.Ala3872Ser
|
|
XM_006720726.3:c.11713G>T
|
XP_006720789.1:p.Ala3905Ser
|
|
XM_006720727.3:c.11470G>T
|
XP_006720790.1:p.Ala3824Ser
|
|
XM_017022695.1:c.11614G>T
|
XP_016878184.1:p.Ala3872Ser
|
|
XM_017022696.1:c.11614G>T
|
XP_016878185.1:p.Ala3872Ser
|
|
XM_017022697.1:c.4894G>T
|
XP_016878186.1:p.Ala1632Ser
|
|
XM_017022698.1:c.4894G>T
|
XP_016878187.1:p.Ala1632Ser
|
|
NM_004667.6:c.11728G>T
MANE Select
|
NP_004658.3:p.Ala3910Ser
|
|