ENST00000307363.10:c.1144-37G>C
MANE Select
|
ENSP00000306920.4:n.1144-37G>C
|
|
ENST00000307363.9:c.1144-37G>C
|
ENSP00000306920.4:n.1144-37G>C
|
|
ENST00000307377.12:c.751-37G>C
|
ENSP00000305920.8:n.751-37G>C
|
|
ENST00000399402.7:c.1054-37G>C
|
ENSP00000382333.2:n.1054-37G>C
|
|
ENST00000461475.5:n.243-37G>C
|
|
|
ENST00000467571.5:n.181-37G>C
|
|
|
ENST00000473477.1:n.176-37G>C
|
|
|
ENST00000482097.5:n.519-37G>C
|
|
|
ENST00000497796.5:n.396-37G>C
|
|
|
NM_000404.2:c.1144-37G>C
|
NP_000395.2:n.1144-37G>C
|
|
NM_000404.3:c.1144-37G>C
|
NP_000395.2:n.1144-37G>C
|
|
NM_001079811.1:c.1054-37G>C
|
NP_001073279.1:n.1054-37G>C
|
|
NM_001079811.2:c.1054-37G>C
|
NP_001073279.1:n.1054-37G>C
|
|
NM_001135602.1:c.751-37G>C
|
NP_001129074.1:n.751-37G>C
|
|
NM_001135602.2:c.751-37G>C
|
NP_001129074.1:n.751-37G>C
|
|
NM_001317040.1:c.1288-37G>C
|
NP_001303969.1:n.1288-37G>C
|
|
XR_001740634.1:n.1543-496C>G
|
|
|
NM_000404.4:c.1144-37G>C
MANE Select
|
NP_000395.3:n.1144-37G>C
|
|
NM_001079811.3:c.1054-37G>C
|
NP_001073279.2:n.1054-37G>C
|
|
NM_001135602.3:c.751-37G>C
|
NP_001129074.2:n.751-37G>C
|
|
NM_001317040.2:c.1288-37G>C
|
NP_001303969.2:n.1288-37G>C
|
|
NM_001393580.1:c.1144-37G>C
|
NP_001380509.1:n.1144-37G>C
|
|