ENST00000281928.9:c.6387+43T>C
MANE Select
|
ENSP00000281928.3:n.6387+43T>C
|
|
ENST00000548784.2:n.2601+43T>C
|
|
|
ENST00000648379.1:n.4755+43T>C
|
|
|
ENST00000648737.1:n.6151+43T>C
|
|
|
ENST00000648762.1:n.1077+43T>C
|
|
|
ENST00000648825.1:n.4572+43T>C
|
|
|
ENST00000648916.1:n.4398+43T>C
|
|
|
ENST00000649607.1:c.4571+43T>C
|
|
|
ENST00000649775.1:c.2718+43T>C
|
|
|
ENST00000650226.1:c.6423+43T>C
|
ENSP00000496981.1:n.6423+43T>C
|
|
ENST00000281928.7:c.6387+43T>C
|
ENSP00000281928.3:n.6387+43T>C
|
|
NM_015335.4:c.6387+43T>C
|
NP_056150.1:n.6387+43T>C
|
|
XM_011538080.1:c.6423+43T>C
|
XP_011536382.1:n.6423+43T>C
|
|
XM_011538081.1:c.6420+43T>C
|
XP_011536383.1:n.6420+43T>C
|
|
XM_011538082.1:c.6393+43T>C
|
XP_011536384.1:n.6393+43T>C
|
|
XM_011538080.2:c.6423+43T>C
|
XP_011536382.1:n.6423+43T>C
|
|
XM_011538081.2:c.6420+43T>C
|
XP_011536383.1:n.6420+43T>C
|
|
XM_011538082.2:c.6393+43T>C
|
XP_011536384.1:n.6393+43T>C
|
|
XM_017019090.1:c.6384+43T>C
|
XP_016874579.1:n.6384+43T>C
|
|
NM_015335.5:c.6387+43T>C
MANE Select
|
NP_056150.1:n.6387+43T>C
|
|