ENST00000225964.10:c.3207+83G>T
MANE Select
|
ENSP00000225964.6:n.3207+83G>T
|
|
ENST00000225964.9:c.3207+83G>T
|
ENSP00000225964.5:n.3207+83G>T
|
|
ENST00000486572.1:n.108G>T
|
|
|
ENST00000511732.1:n.234G>T
|
|
|
NM_000088.3:c.3207+83G>T , LRG_1t1:c.3207+83G>T
|
NP_000079.2:n.3207+83G>T
|
|
XM_005257058.3:c.2937+83G>T
|
XP_005257115.2:n.2937+83G>T
|
|
XM_005257059.3:c.2289+83G>T
|
XP_005257116.2:n.2289+83G>T
|
|
XM_011524341.1:c.3009+83G>T
|
XP_011522643.1:n.3009+83G>T
|
|
XM_005257058.4:c.2937+83G>T
|
XP_005257115.2:n.2937+83G>T
|
|
XM_005257059.4:c.2289+83G>T
|
XP_005257116.2:n.2289+83G>T
|
|
NM_000088.4:c.3207+83G>T
MANE Select
|
NP_000079.2:n.3207+83G>T
|
|