ENST00000288840.10:c.952+17381C>T
MANE Select
|
ENSP00000288840.5:n.952+17381C>T
|
|
ENST00000288840.9:c.952+17381C>T
|
ENSP00000288840.5:n.952+17381C>T
|
|
ENST00000557916.5:c.1084+16739C>T
|
ENSP00000452955.1:n.1084+16739C>T
|
|
ENST00000559931.5:c.256+16739C>T
|
ENSP00000453446.1:n.256+16739C>T
|
|
NM_005585.4:c.952+17381C>T
|
NP_005576.3:n.952+17381C>T
|
|
NR_027654.1:n.2007+16739C>T
|
|
|
XM_011521561.1:c.169+17381C>T
|
XP_011519863.1:n.169+17381C>T
|
|
XR_931825.1:n.2351+17381C>T
|
|
|
XM_011521561.2:c.169+17381C>T
|
XP_011519863.1:n.169+17381C>T
|
|
NM_005585.5:c.952+17381C>T
MANE Select
|
NP_005576.3:n.952+17381C>T
|
|
NR_027654.2:n.2107+16739C>T
|
|
|