ENST00000644269.2:c.1544+239G>C
MANE Select
|
ENSP00000494017.1:n.1544+239G>C
|
|
ENST00000644846.1:c.255+239G>C
|
|
|
ENST00000265715.7:c.1544+239G>C
|
ENSP00000265715.3:n.1544+239G>C
|
|
ENST00000477350.5:n.391+239G>C
|
|
|
ENST00000480841.5:n.393+239G>C
|
|
|
NM_000441.1:c.1544+239G>C
|
NP_000432.1:n.1544+239G>C
|
|
XM_005250425.1:c.1544+239G>C
|
XP_005250482.1:n.1544+239G>C
|
|
XM_005250425.2:c.1544+239G>C
|
XP_005250482.1:n.1544+239G>C
|
|
XM_017012318.1:c.1466+239G>C
|
XP_016867807.1:n.1466+239G>C
|
|
NM_000441.2:c.1544+239G>C
MANE Select
|
NP_000432.1:n.1544+239G>C
|
|