ENST00000248846.10:c.2154+4G>C
MANE Select
|
ENSP00000248846.5:n.2154+4G>C
|
|
ENST00000248846.9:c.2154+4G>C
|
ENSP00000248846.5:n.2154+4G>C
|
|
ENST00000439308.6:c.2154+4G>C
|
ENSP00000397387.2:n.2154+4G>C
|
|
ENST00000473946.1:n.463+4G>C
|
|
|
ENST00000489511.5:n.171+4G>C
|
|
|
ENST00000491449.5:n.461+4G>C
|
|
|
ENST00000498611.5:n.2687+4G>C
|
|
|
NM_020461.3:c.2154+4G>C
|
NP_065194.2:n.2154+4G>C
|
|
XR_938347.1:n.2719+4G>C
|
|
|
XR_938348.1:n.2719+4G>C
|
|
|
XR_001755343.2:n.2723+4G>C
|
|
|
XR_001755344.2:n.2723+4G>C
|
|
|
XR_002958720.1:n.2723+4G>C
|
|
|
XR_938347.2:n.2723+4G>C
|
|
|
NM_020461.4:c.2154+4G>C
MANE Select
|
NP_065194.3:n.2154+4G>C
|
|