ENST00000624552.4:c.14951T>A
|
ENSP00000485357.2:p.Leu4984His
|
|
ENST00000683500.2:c.15008T>A
MANE Select
|
ENSP00000508292.2:p.Leu5003His
|
|
ENST00000623487.1:n.3354T>A
|
|
|
ENST00000624552.3:c.14948T>A
|
ENSP00000485357.1:p.Leu4983His
|
|
NM_001291815.1:c.15008T>A
|
NP_001278744.1:p.Leu5003His
|
|
XM_011518465.1:c.14885T>A
|
XP_011516767.1:p.Leu4962His
|
|
XM_011518466.1:c.14876T>A
|
XP_011516768.1:p.Leu4959His
|
|
XM_011518467.1:c.14831T>A
|
XP_011516769.1:p.Leu4944His
|
|
NM_001291815.2:c.15008T>A
MANE Select
|
NP_001278744.1:p.Leu5003His
|
|
XM_011518465.2:c.14885T>A
|
XP_011516767.1:p.Leu4962His
|
|
XM_011518466.2:c.14876T>A
|
XP_011516768.1:p.Leu4959His
|
|
XM_011518467.2:c.14831T>A
|
XP_011516769.1:p.Leu4944His
|
|
XM_017014585.1:c.11789T>A
|
XP_016870074.1:p.Leu3930His
|
|
XM_017014586.1:c.7586T>A
|
XP_016870075.1:p.Leu2529His
|
|
XR_001746957.1:n.92+160A>T
|
|
|
XR_001746958.1:n.92+160A>T
|
|
|