ENST00000624552.4:c.14968G>T
|
ENSP00000485357.2:p.Val4990Phe
|
|
ENST00000683500.2:c.15025G>T
MANE Select
|
ENSP00000508292.2:p.Val5009Phe
|
|
ENST00000623487.1:n.3371G>T
|
|
|
ENST00000624552.3:c.14965G>T
|
ENSP00000485357.1:p.Val4989Phe
|
|
NM_001291815.1:c.15025G>T
|
NP_001278744.1:p.Val5009Phe
|
|
XM_011518465.1:c.14902G>T
|
XP_011516767.1:p.Val4968Phe
|
|
XM_011518466.1:c.14893G>T
|
XP_011516768.1:p.Val4965Phe
|
|
XM_011518467.1:c.14848G>T
|
XP_011516769.1:p.Val4950Phe
|
|
NM_001291815.2:c.15025G>T
MANE Select
|
NP_001278744.1:p.Val5009Phe
|
|
XM_011518465.2:c.14902G>T
|
XP_011516767.1:p.Val4968Phe
|
|
XM_011518466.2:c.14893G>T
|
XP_011516768.1:p.Val4965Phe
|
|
XM_011518467.2:c.14848G>T
|
XP_011516769.1:p.Val4950Phe
|
|
XM_017014585.1:c.11806G>T
|
XP_016870074.1:p.Val3936Phe
|
|
XM_017014586.1:c.7603G>T
|
XP_016870075.1:p.Val2535Phe
|
|
XR_001746957.1:n.92+143C>A
|
|
|
XR_001746958.1:n.92+143C>A
|
|
|