ENST00000394867.9:n.1424-113G>T
|
|
|
ENST00000688002.1:n.3136-113G>T
|
|
|
ENST00000688751.1:n.121-113G>T
|
|
|
ENST00000689792.1:n.889-113G>T
|
|
|
ENST00000262948.10:c.985-113G>T
MANE Select
|
ENSP00000262948.4:n.985-113G>T
|
|
ENST00000262948.9:c.985-113G>T
|
ENSP00000262948.3:n.985-113G>T
|
|
ENST00000394867.8:c.694-113G>T
|
ENSP00000378336.1:n.694-113G>T
|
|
ENST00000595715.1:n.800-113G>T
|
|
|
ENST00000597263.5:n.170-113G>T
|
|
|
ENST00000599021.1:c.95-113G>T
|
|
|
ENST00000600584.5:n.1545-113G>T
|
|
|
ENST00000601786.5:n.1286-113G>T
|
|
|
NM_030662.3:c.985-113G>T , LRG_750t1:c.985-113G>T
|
NP_109587.1:n.985-113G>T
|
|
XM_006722799.2:c.706-113G>T
|
XP_006722862.1:n.706-113G>T
|
|
XM_011528133.1:c.415-113G>T
|
XP_011526435.1:n.415-113G>T
|
|
XM_017026989.1:c.985-113G>T
|
XP_016882478.1:n.985-113G>T
|
|
XM_017026990.1:c.706-113G>T
|
XP_016882479.1:n.706-113G>T
|
|
NM_030662.4:c.985-113G>T
MANE Select
|
NP_109587.1:n.985-113G>T
|
|