ENST00000508233.6:c.417+238G>T
|
ENSP00000422973.2:n.417+238G>T
|
|
ENST00000614857.5:c.540+238G>T
|
ENSP00000477824.2:n.540+238G>T
|
|
ENST00000681973.1:n.767+238G>T
|
|
|
ENST00000682026.1:n.493+238G>T
|
|
|
ENST00000682448.1:n.2026+238G>T
|
|
|
ENST00000682554.1:n.1988+238G>T
|
|
|
ENST00000682599.1:n.3028+238G>T
|
|
|
ENST00000682627.1:n.460+238G>T
|
|
|
ENST00000682865.1:n.824+238G>T
|
|
|
ENST00000683087.1:n.554+238G>T
|
|
|
ENST00000683168.1:n.1294+238G>T
|
|
|
ENST00000683620.1:n.1722+238G>T
|
|
|
ENST00000684106.1:n.2790+238G>T
|
|
|
ENST00000684450.1:n.1599+238G>T
|
|
|
ENST00000684710.1:n.1831+238G>T
|
|
|
ENST00000395080.8:c.540+238G>T
MANE Select
|
ENSP00000378517.3:n.540+238G>T
|
|
ENST00000237623.11:c.498+238G>T
|
ENSP00000237623.7:n.498+238G>T
|
|
ENST00000360804.4:c.459+238G>T
|
ENSP00000354042.4:n.459+238G>T
|
|
ENST00000395080.7:c.540+238G>T
|
ENSP00000378517.3:n.540+238G>T
|
|
ENST00000508233.5:c.417+238G>T
|
ENSP00000422973.1:n.417+238G>T
|
|
ENST00000509659.5:n.829+238G>T
|
|
|
ENST00000614857.4:c.474+238G>T
|
ENSP00000477824.1:n.474+238G>T
|
|
NM_000582.2:c.498+238G>T
|
NP_000573.1:n.498+238G>T
|
|
NM_001040058.1:c.540+238G>T
|
NP_001035147.1:n.540+238G>T
|
|
NM_001040060.1:c.459+238G>T
|
NP_001035149.1:n.459+238G>T
|
|
NM_001251829.1:c.417+238G>T
|
NP_001238758.1:n.417+238G>T
|
|
NM_001251830.1:c.579+238G>T
|
NP_001238759.1:n.579+238G>T
|
|
NM_001040058.2:c.540+238G>T
MANE Select
|
NP_001035147.1:n.540+238G>T
|
|
NM_000582.3:c.498+238G>T
|
NP_000573.1:n.498+238G>T
|
|
NM_001040060.2:c.459+238G>T
|
NP_001035149.1:n.459+238G>T
|
|
NM_001251829.2:c.417+238G>T
|
NP_001238758.1:n.417+238G>T
|
|
NM_001251830.2:c.579+238G>T
|
NP_001238759.1:n.579+238G>T
|
|