NM_014181.3:c.14T>C
(LGALSL)
MANE Select
|
NP_054900.2:p.Val5Ala
|
ENST00000238875.10:c.14T>C
(LGALSL)
MANE Select
|
ENSP00000238875.4:p.Val5Ala
|
NM_014181.2:c.14T>C
(LGALSL)
|
NP_054900.2:p.Val5Ala
|
ENST00000238875.9:c.14T>C
(LGALSL)
|
ENSP00000238875.4:p.Val5Ala
|
ENST00000409537.2:c.14T>C
(LGALSL)
|
ENSP00000386242.2:p.Val5Ala
|
ENST00000420552.5:c.14T>C
(LGALSL)
|
ENSP00000407486.1:p.Val5Ala
|
ENST00000462737.1:c.14T>C
(LGALSL)
|
ENSP00000476226.1:p.Val5Ala
|
ENST00000464281.5:c.14T>C
(LGALSL)
|
ENSP00000475643.1:p.Val5Ala
|
XR_002959392.1:n.728A>G
(LGALSL-DT)
|
|