|
ENST00000513939.6:c.1449C>T
(GCLC)
|
ENSP00000424211.2:p.Asp483=
|
|
|
ENST00000616923.5:c.1404C>T
(GCLC)
|
ENSP00000482756.2:p.Asp468=
|
|
|
ENST00000643939.1:c.1569C>T
(GCLC)
|
ENSP00000495686.1:p.Asp523=
|
|
|
ENST00000650454.1:c.1563C>T
(GCLC)
MANE Select
|
ENSP00000497574.1:p.Asp521=
|
|
|
ENST00000229416.10:c.1563C>T
(GCLC)
|
ENSP00000229416.6:p.Asp521=
|
|
|
ENST00000504353.1:n.532C>T
(GCLC)
|
|
|
|
ENST00000509541.5:n.2008C>T
(GCLC)
|
|
|
|
ENST00000510837.5:n.441C>T
(GCLC)
|
|
|
|
ENST00000515580.1:n.1086C>T
(GCLC)
|
|
|
|
ENST00000616923.4:c.1449C>T
(GCLC)
|
ENSP00000482756.1:p.Asp483=
|
|
|
NM_001197115.1:c.1449C>T
(GCLC)
|
NP_001184044.1:p.Asp483=
|
|
|
NM_001498.3:c.1563C>T
(GCLC)
|
NP_001489.1:p.Asp521=
|
|
|
XR_926888.1:n.87-5889G>A
(GCLC-AS1)
|
|
|
|
XR_926889.1:n.56-5889G>A
(GCLC-AS1)
|
|
|
|
NM_001498.4:c.1563C>T
(GCLC)
MANE Select
|
NP_001489.1:p.Asp521=
|
|
|
XM_017010749.1:c.852C>T
(GCLC)
|
XP_016866238.1:p.Asp284=
|
|
|
NM_001197115.2:c.1449C>T
(GCLC)
|
NP_001184044.1:p.Asp483=
|
|
