ENST00000512905.6:c.16T>A
|
|
|
ENST00000647941.2:c.1130T>A
MANE Select
|
ENSP00000497326.1:p.Phe377Tyr
|
|
ENST00000264193.2:c.1130T>A
|
ENSP00000264193.2:p.Phe377Tyr
|
|
ENST00000510489.1:n.380T>A
|
|
|
ENST00000512905.5:c.16T>A
|
|
|
NM_000097.5:c.1130T>A
|
NP_000088.3:p.Phe377Tyr
|
|
XM_005247125.3:c.1130T>A
|
XP_005247182.1:p.Phe377Tyr
|
|
NM_000097.7:c.1130T>A
MANE Select
|
NP_000088.3:p.Phe377Tyr
|
|
XM_005247125.4:c.1130T>A
|
XP_005247182.1:p.Phe377Tyr
|
|
XR_001740025.2:n.1301T>A
|
|
|
XR_001740026.1:n.1865T>A
|
|
|
XR_001740027.1:n.1405T>A
|
|
|
XR_001740028.1:n.1371T>A
|
|
|