ENST00000624552.4:c.14893C>T
|
ENSP00000485357.2:p.Gln4965Ter
|
|
ENST00000683500.2:c.14950C>T
MANE Select
|
ENSP00000508292.2:p.Gln4984Ter
|
|
ENST00000623487.1:n.3296C>T
|
|
|
ENST00000624552.3:c.14890C>T
|
ENSP00000485357.1:p.Gln4964Ter
|
|
NM_001291815.1:c.14950C>T
|
NP_001278744.1:p.Gln4984Ter
|
|
XM_011518465.1:c.14827C>T
|
XP_011516767.1:p.Gln4943Ter
|
|
XM_011518466.1:c.14818C>T
|
XP_011516768.1:p.Gln4940Ter
|
|
XM_011518467.1:c.14773C>T
|
XP_011516769.1:p.Gln4925Ter
|
|
NM_001291815.2:c.14950C>T
MANE Select
|
NP_001278744.1:p.Gln4984Ter
|
|
XM_011518465.2:c.14827C>T
|
XP_011516767.1:p.Gln4943Ter
|
|
XM_011518466.2:c.14818C>T
|
XP_011516768.1:p.Gln4940Ter
|
|
XM_011518467.2:c.14773C>T
|
XP_011516769.1:p.Gln4925Ter
|
|
XM_017014585.1:c.11731C>T
|
XP_016870074.1:p.Gln3911Ter
|
|
XM_017014586.1:c.7528C>T
|
XP_016870075.1:p.Gln2510Ter
|
|
XR_001746957.1:n.92+218G>A
|
|
|
XR_001746958.1:n.92+218G>A
|
|
|