ENST00000513939.6:c.1083+1G>C
|
ENSP00000424211.2:n.1083+1G>C
|
|
ENST00000616923.5:c.1038+1G>C
|
ENSP00000482756.2:n.1038+1G>C
|
|
ENST00000643939.1:c.1203+1G>C
|
ENSP00000495686.1:n.1203+1G>C
|
|
ENST00000650454.1:c.1197+1G>C
MANE Select
|
ENSP00000497574.1:n.1197+1G>C
|
|
ENST00000229416.10:c.1197+1G>C
|
ENSP00000229416.6:n.1197+1G>C
|
|
ENST00000504353.1:n.166+1G>C
|
|
|
ENST00000509541.5:n.1642+1G>C
|
|
|
ENST00000616923.4:c.1083+1G>C
|
ENSP00000482756.1:n.1083+1G>C
|
|
NM_001197115.1:c.1083+1G>C
|
NP_001184044.1:n.1083+1G>C
|
|
NM_001498.3:c.1197+1G>C
|
NP_001489.1:n.1197+1G>C
|
|
NM_001498.4:c.1197+1G>C
MANE Select
|
NP_001489.1:n.1197+1G>C
|
|
XM_017010749.1:c.486+1G>C
|
XP_016866238.1:n.486+1G>C
|
|
NM_001197115.2:c.1083+1G>C
|
NP_001184044.1:n.1083+1G>C
|
|