ENST00000261609.13:c.11841T>C
MANE Select
|
ENSP00000261609.8:p.Ser3947=
|
|
ENST00000650509.1:c.3552T>C
|
ENSP00000496936.1:p.Ser1184=
|
|
ENST00000261609.11:c.11841T>C
|
ENSP00000261609.7:p.Ser3947=
|
|
NM_004667.5:c.11841T>C
|
NP_004658.3:p.Ser3947=
|
|
XM_005268276.3:c.11727T>C
|
XP_005268333.1:p.Ser3909=
|
|
XM_005268277.3:c.11727T>C
|
XP_005268334.1:p.Ser3909=
|
|
XM_006720726.2:c.11826T>C
|
XP_006720789.1:p.Ser3942=
|
|
XM_006720727.2:c.11583T>C
|
XP_006720790.1:p.Ser3861=
|
|
XM_011522131.1:c.11358T>C
|
XP_011520433.1:p.Ser3786=
|
|
XM_011522132.1:c.9357T>C
|
XP_011520434.1:p.Ser3119=
|
|
XM_011522133.1:c.8586T>C
|
XP_011520435.1:p.Ser2862=
|
|
XM_011522134.1:c.5958T>C
|
XP_011520436.1:p.Ser1986=
|
|
XM_005268276.5:c.11727T>C
|
XP_005268333.1:p.Ser3909=
|
|
XM_006720726.3:c.11826T>C
|
XP_006720789.1:p.Ser3942=
|
|
XM_006720727.3:c.11583T>C
|
XP_006720790.1:p.Ser3861=
|
|
XM_017022695.1:c.11727T>C
|
XP_016878184.1:p.Ser3909=
|
|
XM_017022696.1:c.11727T>C
|
XP_016878185.1:p.Ser3909=
|
|
XM_017022697.1:c.5007T>C
|
XP_016878186.1:p.Ser1669=
|
|
XM_017022698.1:c.5007T>C
|
XP_016878187.1:p.Ser1669=
|
|
NM_004667.6:c.11841T>C
MANE Select
|
NP_004658.3:p.Ser3947=
|
|