ENST00000700061.1:c.562T>A
|
|
|
ENST00000700062.1:c.562T>A
|
|
|
ENST00000700065.1:n.2478T>A
|
|
|
ENST00000700066.1:c.1982T>A
|
ENSP00000514780.1:p.Leu661Ter
|
|
ENST00000281513.10:c.2465T>A
MANE Select
|
ENSP00000281513.5:p.Leu822Ter
|
|
ENST00000281513.9:c.2465T>A
|
ENSP00000281513.5:p.Leu822Ter
|
|
NM_015909.3:c.2465T>A
|
NP_056993.2:p.Leu822Ter
|
|
NR_052013.2:n.2509T>A
|
|
|
XM_011510357.1:c.2336T>A
|
XP_011508659.1:p.Leu779Ter
|
|
XM_011510358.1:c.2465T>A
|
XP_011508660.1:p.Leu822Ter
|
|
XM_011510359.1:c.1826T>A
|
XP_011508661.1:p.Leu609Ter
|
|
XM_011510360.1:c.266T>A
|
XP_011508662.1:p.Leu89Ter
|
|
XM_011510361.1:c.257T>A
|
XP_011508663.1:p.Leu86Ter
|
|
XM_011510357.2:c.2336T>A
|
XP_011508659.1:p.Leu779Ter
|
|
XM_011510358.2:c.2465T>A
|
XP_011508660.1:p.Leu822Ter
|
|
XM_011510360.2:c.266T>A
|
XP_011508662.1:p.Leu89Ter
|
|
XM_011510361.2:c.257T>A
|
XP_011508663.1:p.Leu86Ter
|
|
XM_017004317.1:c.2465T>A
|
XP_016859806.1:p.Leu822Ter
|
|
XM_024452961.1:c.1826T>A
|
XP_024308729.1:p.Leu609Ter
|
|
NM_015909.4:c.2465T>A
MANE Select
|
NP_056993.2:p.Leu822Ter
|
|
NR_052013.3:n.2495T>A
|
|
|