ENST00000426263.10:c.486G>C
MANE Select
|
ENSP00000416293.2:p.Leu162=
|
|
ENST00000674765.1:c.486G>C
|
ENSP00000501811.1:p.Leu162=
|
|
ENST00000675112.1:n.509G>C
|
|
|
ENST00000676254.1:n.935G>C
|
|
|
ENST00000426263.7:c.486G>C
|
ENSP00000416293.2:p.Leu162=
|
|
ENST00000439722.2:c.365G>C
|
ENSP00000395521.2:n.365G>C
|
|
ENST00000475162.3:c.385G>C
|
|
|
ENST00000625233.2:n.694G>C
|
|
|
ENST00000630287.2:c.486G>C
|
ENSP00000486694.1:p.Leu162=
|
|
NM_006516.2:c.486G>C
|
NP_006507.2:p.Leu162=
|
|
NM_006516.3:c.486G>C
|
NP_006507.2:p.Leu162=
|
|
NM_006516.4:c.486G>C
MANE Select
|
NP_006507.2:p.Leu162=
|
|