ENST00000456935.7:c.1830+42A>T
MANE Select
|
ENSP00000395473.2:n.1830+42A>T
|
|
ENST00000221363.8:c.1827+42A>T
|
ENSP00000221363.4:n.1827+42A>T
|
|
ENST00000433513.5:n.436+42A>T
|
|
|
ENST00000456935.6:c.1830+42A>T
|
ENSP00000395473.2:n.1830+42A>T
|
|
ENST00000466794.5:n.2420+42A>T
|
|
|
ENST00000593686.1:c.423+42A>T
|
|
|
ENST00000595880.5:n.427+42A>T
|
|
|
ENST00000596591.1:c.194+42A>T
|
|
|
NM_000528.3:c.1830+42A>T
|
NP_000519.2:n.1830+42A>T
|
|
NM_001173498.1:c.1827+42A>T
|
NP_001166969.1:n.1827+42A>T
|
|
XM_005259913.1:c.1833+42A>T
|
XP_005259970.1:n.1833+42A>T
|
|
XM_011528017.1:c.729+42A>T
|
XP_011526319.1:n.729+42A>T
|
|
XM_005259913.2:c.1833+42A>T
|
XP_005259970.1:n.1833+42A>T
|
|
XM_024451518.1:c.729+42A>T
|
XP_024307286.1:n.729+42A>T
|
|
NM_000528.4:c.1830+42A>T
MANE Select
|
NP_000519.2:n.1830+42A>T
|
|
NM_001173498.2:c.1827+42A>T
|
NP_001166969.1:n.1827+42A>T
|
|