ENST00000261609.13:c.11969T>C
MANE Select
|
ENSP00000261609.8:p.Leu3990Ser
|
|
ENST00000650509.1:c.3680T>C
|
ENSP00000496936.1:p.Leu1227Ser
|
|
ENST00000261609.11:c.11969T>C
|
ENSP00000261609.7:p.Leu3990Ser
|
|
NM_004667.5:c.11969T>C
|
NP_004658.3:p.Leu3990Ser
|
|
XM_005268276.3:c.11855T>C
|
XP_005268333.1:p.Leu3952Ser
|
|
XM_005268277.3:c.11855T>C
|
XP_005268334.1:p.Leu3952Ser
|
|
XM_006720726.2:c.11954T>C
|
XP_006720789.1:p.Leu3985Ser
|
|
XM_006720727.2:c.11711T>C
|
XP_006720790.1:p.Leu3904Ser
|
|
XM_011522131.1:c.11486T>C
|
XP_011520433.1:p.Leu3829Ser
|
|
XM_011522132.1:c.9485T>C
|
XP_011520434.1:p.Leu3162Ser
|
|
XM_011522133.1:c.8714T>C
|
XP_011520435.1:p.Leu2905Ser
|
|
XM_011522134.1:c.6086T>C
|
XP_011520436.1:p.Leu2029Ser
|
|
XM_005268276.5:c.11855T>C
|
XP_005268333.1:p.Leu3952Ser
|
|
XM_006720726.3:c.11954T>C
|
XP_006720789.1:p.Leu3985Ser
|
|
XM_006720727.3:c.11711T>C
|
XP_006720790.1:p.Leu3904Ser
|
|
XM_017022695.1:c.11855T>C
|
XP_016878184.1:p.Leu3952Ser
|
|
XM_017022696.1:c.11855T>C
|
XP_016878185.1:p.Leu3952Ser
|
|
XM_017022697.1:c.5135T>C
|
XP_016878186.1:p.Leu1712Ser
|
|
XM_017022698.1:c.5135T>C
|
XP_016878187.1:p.Leu1712Ser
|
|
NM_004667.6:c.11969T>C
MANE Select
|
NP_004658.3:p.Leu3990Ser
|
|