ENST00000624552.4:c.14912T>G
|
ENSP00000485357.2:p.Leu4971Arg
|
|
ENST00000683500.2:c.14969T>G
MANE Select
|
ENSP00000508292.2:p.Leu4990Arg
|
|
ENST00000623487.1:n.3315T>G
|
|
|
ENST00000624552.3:c.14909T>G
|
ENSP00000485357.1:p.Leu4970Arg
|
|
NM_001291815.1:c.14969T>G
|
NP_001278744.1:p.Leu4990Arg
|
|
XM_011518465.1:c.14846T>G
|
XP_011516767.1:p.Leu4949Arg
|
|
XM_011518466.1:c.14837T>G
|
XP_011516768.1:p.Leu4946Arg
|
|
XM_011518467.1:c.14792T>G
|
XP_011516769.1:p.Leu4931Arg
|
|
NM_001291815.2:c.14969T>G
MANE Select
|
NP_001278744.1:p.Leu4990Arg
|
|
XM_011518465.2:c.14846T>G
|
XP_011516767.1:p.Leu4949Arg
|
|
XM_011518466.2:c.14837T>G
|
XP_011516768.1:p.Leu4946Arg
|
|
XM_011518467.2:c.14792T>G
|
XP_011516769.1:p.Leu4931Arg
|
|
XM_017014585.1:c.11750T>G
|
XP_016870074.1:p.Leu3917Arg
|
|
XM_017014586.1:c.7547T>G
|
XP_016870075.1:p.Leu2516Arg
|
|
XR_001746957.1:n.92+199A>C
|
|
|
XR_001746958.1:n.92+199A>C
|
|
|