ENST00000299506.3:c.253+19C>T
MANE Select
|
ENSP00000299506.3:n.253+19C>T
|
|
ENST00000299506.2:c.253+19C>T
|
ENSP00000299506.2:n.253+19C>T
|
|
ENST00000305253.8:c.418+19C>T
|
ENSP00000305426.4:n.418+19C>T
|
|
ENST00000534099.5:c.271+19C>T
|
ENSP00000434400.1:n.271+19C>T
|
|
NM_003320.4:c.418+19C>T
|
NP_003311.2:n.418+19C>T
|
|
NM_177972.2:c.253+19C>T
|
NP_813977.1:n.253+19C>T
|
|
XM_005253109.2:c.379+19C>T
|
XP_005253166.1:n.379+19C>T
|
|
XM_011520344.1:c.289+19C>T
|
XP_011518646.1:n.289+19C>T
|
|
XM_005253109.3:c.379+19C>T
|
XP_005253166.1:n.379+19C>T
|
|
XM_011520344.2:c.289+19C>T
|
XP_011518646.1:n.289+19C>T
|
|
NM_177972.3:c.253+19C>T
MANE Select
|
NP_813977.1:n.253+19C>T
|
|
NM_003320.5:c.418+19C>T
|
NP_003311.2:n.418+19C>T
|
|