ENST00000281928.9:c.4956-27G>T
MANE Select
|
ENSP00000281928.3:n.4956-27G>T
|
|
ENST00000549786.2:c.4384-27G>T
|
|
|
ENST00000648379.1:n.3324-27G>T
|
|
|
ENST00000648737.1:n.4720-27G>T
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|
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ENST00000648825.1:n.1696-27G>T
|
|
|
ENST00000648916.1:n.2967-27G>T
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|
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ENST00000649146.1:n.2172G>T
|
|
|
ENST00000649607.1:c.3140-27G>T
|
|
|
ENST00000649775.1:c.1453-35G>T
|
|
|
ENST00000650226.1:c.4956-27G>T
|
ENSP00000496981.1:n.4956-27G>T
|
|
ENST00000281928.7:c.4956-27G>T
|
ENSP00000281928.3:n.4956-27G>T
|
|
ENST00000549786.1:c.320-27G>T
|
|
|
NM_015335.4:c.4956-27G>T
|
NP_056150.1:n.4956-27G>T
|
|
XM_011538080.1:c.4956-27G>T
|
XP_011536382.1:n.4956-27G>T
|
|
XM_011538081.1:c.4953-27G>T
|
XP_011536383.1:n.4953-27G>T
|
|
XM_011538082.1:c.4926-27G>T
|
XP_011536384.1:n.4926-27G>T
|
|
XM_011538080.2:c.4956-27G>T
|
XP_011536382.1:n.4956-27G>T
|
|
XM_011538081.2:c.4953-27G>T
|
XP_011536383.1:n.4953-27G>T
|
|
XM_011538082.2:c.4926-27G>T
|
XP_011536384.1:n.4926-27G>T
|
|
XM_017019090.1:c.4953-27G>T
|
XP_016874579.1:n.4953-27G>T
|
|
NM_015335.5:c.4956-27G>T
MANE Select
|
NP_056150.1:n.4956-27G>T
|
|