ENST00000624552.4:c.14954C>A
|
ENSP00000485357.2:p.Thr4985Asn
|
|
ENST00000683500.2:c.15011C>A
MANE Select
|
ENSP00000508292.2:p.Thr5004Asn
|
|
ENST00000623487.1:n.3357C>A
|
|
|
ENST00000624552.3:c.14951C>A
|
ENSP00000485357.1:p.Thr4984Asn
|
|
NM_001291815.1:c.15011C>A
|
NP_001278744.1:p.Thr5004Asn
|
|
XM_011518465.1:c.14888C>A
|
XP_011516767.1:p.Thr4963Asn
|
|
XM_011518466.1:c.14879C>A
|
XP_011516768.1:p.Thr4960Asn
|
|
XM_011518467.1:c.14834C>A
|
XP_011516769.1:p.Thr4945Asn
|
|
NM_001291815.2:c.15011C>A
MANE Select
|
NP_001278744.1:p.Thr5004Asn
|
|
XM_011518465.2:c.14888C>A
|
XP_011516767.1:p.Thr4963Asn
|
|
XM_011518466.2:c.14879C>A
|
XP_011516768.1:p.Thr4960Asn
|
|
XM_011518467.2:c.14834C>A
|
XP_011516769.1:p.Thr4945Asn
|
|
XM_017014585.1:c.11792C>A
|
XP_016870074.1:p.Thr3931Asn
|
|
XM_017014586.1:c.7589C>A
|
XP_016870075.1:p.Thr2530Asn
|
|
XR_001746957.1:n.92+157G>T
|
|
|
XR_001746958.1:n.92+157G>T
|
|
|