ENST00000281928.9:c.5915T>A
MANE Select
|
ENSP00000281928.3:p.Phe1972Tyr
|
|
ENST00000548784.2:n.2129T>A
|
|
|
ENST00000648379.1:n.4283T>A
|
|
|
ENST00000648737.1:n.5679T>A
|
|
|
ENST00000648825.1:n.4100T>A
|
|
|
ENST00000648916.1:n.3926T>A
|
|
|
ENST00000649607.1:c.4099T>A
|
|
|
ENST00000649775.1:c.2404T>A
|
|
|
ENST00000650226.1:c.5951T>A
|
ENSP00000496981.1:p.Phe1984Tyr
|
|
ENST00000281928.7:c.5915T>A
|
ENSP00000281928.3:p.Phe1972Tyr
|
|
ENST00000548784.1:n.413T>A
|
|
|
ENST00000552447.1:c.528T>A
|
|
|
NM_015335.4:c.5915T>A
|
NP_056150.1:p.Phe1972Tyr
|
|
XM_011538080.1:c.5951T>A
|
XP_011536382.1:p.Phe1984Tyr
|
|
XM_011538081.1:c.5948T>A
|
XP_011536383.1:p.Phe1983Tyr
|
|
XM_011538082.1:c.5921T>A
|
XP_011536384.1:p.Phe1974Tyr
|
|
XM_011538080.2:c.5951T>A
|
XP_011536382.1:p.Phe1984Tyr
|
|
XM_011538081.2:c.5948T>A
|
XP_011536383.1:p.Phe1983Tyr
|
|
XM_011538082.2:c.5921T>A
|
XP_011536384.1:p.Phe1974Tyr
|
|
XM_017019090.1:c.5912T>A
|
XP_016874579.1:p.Phe1971Tyr
|
|
NM_015335.5:c.5915T>A
MANE Select
|
NP_056150.1:p.Phe1972Tyr
|
|