ENST00000624552.4:c.14852G>C
|
ENSP00000485357.2:p.Arg4951Pro
|
|
ENST00000683500.2:c.14909G>C
MANE Select
|
ENSP00000508292.2:p.Arg4970Pro
|
|
ENST00000623487.1:n.3255G>C
|
|
|
ENST00000624552.3:c.14849G>C
|
ENSP00000485357.1:p.Arg4950Pro
|
|
NM_001291815.1:c.14909G>C
|
NP_001278744.1:p.Arg4970Pro
|
|
XM_011518465.1:c.14786G>C
|
XP_011516767.1:p.Arg4929Pro
|
|
XM_011518466.1:c.14777G>C
|
XP_011516768.1:p.Arg4926Pro
|
|
XM_011518467.1:c.14732G>C
|
XP_011516769.1:p.Arg4911Pro
|
|
NM_001291815.2:c.14909G>C
MANE Select
|
NP_001278744.1:p.Arg4970Pro
|
|
XM_011518465.2:c.14786G>C
|
XP_011516767.1:p.Arg4929Pro
|
|
XM_011518466.2:c.14777G>C
|
XP_011516768.1:p.Arg4926Pro
|
|
XM_011518467.2:c.14732G>C
|
XP_011516769.1:p.Arg4911Pro
|
|
XM_017014585.1:c.11690G>C
|
XP_016870074.1:p.Arg3897Pro
|
|
XM_017014586.1:c.7487G>C
|
XP_016870075.1:p.Arg2496Pro
|
|
XR_001746957.1:n.92+259C>G
|
|
|
XR_001746958.1:n.92+259C>G
|
|
|