ENST00000302103.6:c.*8003G>C
MANE Select
|
ENSP00000302599.4:n.*8003G>C
|
|
ENST00000302103.5:c.*8003G>C
|
ENSP00000302599.4:n.*8003G>C
|
|
NM_006581.3:c.*8003G>C
|
NP_006572.2:n.*8003G>C
|
|
XR_942796.1:n.411-9223C>G
|
|
|
XR_942797.1:n.218-9223C>G
|
|
|
XR_942798.1:n.224-9223C>G
|
|
|
XR_942799.1:n.232-9223C>G
|
|
|
XR_942800.1:n.573-9223C>G
|
|
|
XM_011535383.2:c.*8003G>C
|
XP_011533685.1:n.*8003G>C
|
|
XM_011535385.2:c.*8003G>C
|
XP_011533687.1:n.*8003G>C
|
|
XM_017010188.1:c.*8003G>C
|
XP_016865677.1:n.*8003G>C
|
|
XM_017010190.1:c.*8003G>C
|
XP_016865679.1:n.*8003G>C
|
|
NM_006581.4:c.*8003G>C
MANE Select
|
NP_006572.2:n.*8003G>C
|
|