ENST00000697630.1:n.1458A>C
|
|
|
ENST00000697631.1:c.471A>C
|
ENSP00000513363.1:p.Leu157=
|
|
ENST00000697632.1:c.-283A>C
|
ENSP00000513364.1:n.-283A>C
|
|
ENST00000348564.11:c.273A>C
|
ENSP00000306782.7:p.Leu91=
|
|
ENST00000367379.6:c.273A>C
|
ENSP00000356349.2:p.Leu91=
|
|
ENST00000442510.8:c.756A>C
MANE Select
|
ENSP00000411355.3:p.Leu252=
|
|
ENST00000643513.1:c.414A>C
|
ENSP00000494132.1:p.Leu138=
|
|
ENST00000348564.10:c.273A>C
|
ENSP00000306782.7:p.Leu91=
|
|
ENST00000367367.8:c.558A>C
|
ENSP00000356337.5:p.Leu186=
|
|
ENST00000367379.5:c.273A>C
|
ENSP00000356349.2:p.Leu91=
|
|
ENST00000442510.6:c.756A>C
|
ENSP00000411355.3:p.Leu252=
|
|
ENST00000529828.5:c.612A>C
|
ENSP00000469141.1:p.Leu204=
|
|
ENST00000530727.5:c.414A>C
|
ENSP00000433536.2:p.Leu138=
|
|
NM_002838.4:c.756A>C
|
NP_002829.3:p.Leu252=
|
|
NM_080921.3:c.273A>C
|
NP_563578.2:p.Leu91=
|
|
XM_006711472.2:c.612A>C
|
XP_006711535.1:p.Leu204=
|
|
XM_006711473.2:c.558A>C
|
XP_006711536.1:p.Leu186=
|
|
XM_006711474.2:c.414A>C
|
XP_006711537.1:p.Leu138=
|
|
XM_006711472.4:c.612A>C
|
XP_006711535.1:p.Leu204=
|
|
XM_006711473.3:c.558A>C
|
XP_006711536.1:p.Leu186=
|
|
XM_006711474.3:c.414A>C
|
XP_006711537.1:p.Leu138=
|
|
NM_002838.5:c.756A>C
MANE Select
|
NP_002829.3:p.Leu252=
|
|
NM_080921.4:c.273A>C
|
NP_563578.2:p.Leu91=
|
|