ENST00000539276.7:c.2607+99G>C
MANE Select
|
ENSP00000440045.2:n.2607+99G>C
|
|
ENST00000308664.10:c.2607+99G>C
|
ENSP00000311186.6:n.2607+99G>C
|
|
ENST00000377685.9:c.*2447+99G>C
|
ENSP00000366913.4:n.*2447+99G>C
|
|
ENST00000539276.6:c.2607+99G>C
|
ENSP00000440045.2:n.2607+99G>C
|
|
ENST00000547792.1:n.364G>C
|
|
|
ENST00000548169.2:c.2278+99G>C
|
|
|
NM_001681.3:c.2607+99G>C
|
NP_001672.1:n.2607+99G>C
|
|
NM_170665.3:c.2607+99G>C
|
NP_733765.1:n.2607+99G>C
|
|
XM_005253888.1:c.2607+99G>C
|
XP_005253945.1:n.2607+99G>C
|
|
XM_011538402.1:c.2607+99G>C
|
XP_011536704.1:n.2607+99G>C
|
|
XR_243009.1:n.2613+99G>C
|
|
|
XM_005253888.3:c.2607+99G>C
|
XP_005253945.1:n.2607+99G>C
|
|
XM_011538402.3:c.2607+99G>C
|
XP_011536704.1:n.2607+99G>C
|
|
XR_002957329.1:n.2613+99G>C
|
|
|
XR_243009.3:n.2613+99G>C
|
|
|
NM_170665.4:c.2607+99G>C
MANE Select
|
NP_733765.1:n.2607+99G>C
|
|
NM_001681.4:c.2607+99G>C
|
NP_001672.1:n.2607+99G>C
|
|